JP2005290225A - Lubricating oil composition for paper machine - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a lubricating oil composition for paper machines having simultaneously excellent heat and abrasion resistances and anti-corrosion as a lubricating oil for the paper machines corresponding to the development of the paper machines in recent years. <P>SOLUTION: A lubricating oil composition for the paper machines obtained by compounding (A) a phosphorus-containing carboxylic acid compound and/or (B) a phosphorothionate with at least one kind selected from mineral oils, oils and fats and synthetic oils as a base oil is provided. (A) The phosphorus-containing carboxylic acid compound may contain both a carboxyl group and a phosphorus atom in the same molecule and a phosphorylated carboxylic acid is preferable. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a lubricating oil for a paper machine, and more particularly to a lubricating oil composition for a paper machine that simultaneously satisfies heat resistance, wear resistance, and corrosion resistance.

  A paper machine has a process of making paper and then drying the paper, but the conventional paper machine has a relatively long drying time and a low drying temperature. However, in recent paper machines, the time required for the drying process has been shortened from the improvement of production efficiency, and as a result, the drying temperature has become very high, and the heat resistance requirement for the lubricating oil used in the paper machine is Similarly, the required level of wear resistance for the lubricating oil is also increasing. In addition, paper machines use strongly acidic white water when making paper, but since white water tends to corrode metals, lubricating oil for paper machines is also required to prevent machine corrosion by these white water. It has been. As described above, the lubricating oil for paper machines has high required performance such as heat resistance, wear resistance and corrosion resistance.

Here, conventional oil pressures for paper machines are generally used for improving wear resistance, but extreme pressure agents are generally used. It tends to occur. Therefore, it is conceivable to use a large amount of metallic detergents and ashless dispersants in order to suppress sludge. However, if these are used, problems such as reduced corrosion resistance and corrosion of the paper machine body may occur. As a result, it has been difficult to satisfy all of the required performances of heat resistance, wear resistance and corrosion resistance. For example, Patent Document 1 proposes a paper machine lubricating oil that is excellent in heat resistance, wear resistance, and corrosion resistance, but it is not always satisfactory.
JP 2002-97485 A

  The present invention provides a lubricating oil composition for a paper machine that is excellent in heat resistance, wear resistance and corrosion resistance at the same time.

As a result of intensive studies to solve the above object, the present inventors have found that the above-mentioned problems can be solved by adding a phosphorus-containing carboxylic acid compound and / or phosphorothioate to a predetermined base oil, The present invention has been completed.
That is, the present invention is a paper machine lubrication comprising at least one selected from mineral oil, fat and oil and synthetic oil as a base oil and containing (A) a phosphorus-containing carboxylic acid compound and / or (B) phosphorothionate. It relates to an oil composition.

  The lubricating oil composition for paper machine of the present invention is excellent in heat resistance, wear resistance and corrosion resistance at the same time.

In the lubricating oil composition for paper machine of the present invention, at least one selected from mineral oil, fats and oils and synthetic oils is used as the base oil.
Here, as mineral oil, solvent debris, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, hydrorefining is performed on the lubricating oil fraction obtained by atmospheric distillation and vacuum distillation of crude oil. Examples thereof include paraffinic or naphthenic mineral oils obtained by applying a suitable combination of one or more purification means such as sulfuric acid washing and clay treatment. Further, it is also possible to use a wax isomerized base oil, a base oil produced by a technique for isomerizing GTL WAX (Gas Liquid Wax), and the like.
Examples of the fats and oils include beef tallow, lard, sunflower oil, soybean oil, rapeseed oil, rice bran oil, coconut oil, palm oil, palm kernel oil, and hydrogenated products thereof.

Synthetic oils include, for example, poly α-olefins (ethylene-propylene copolymer, polybutene, 1-octene oligomer, 1-decene oligomer, and hydrides thereof), alkylbenzene, alkylnaphthalene, monoester (butyl). Stearate, octyl laurate), diester (ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, di-2-ethylhexyl sepacate, etc.), polyester (trimellitic acid ester, etc.), polyol ester (Trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol-2-ethylhexanoate, pentaerythritol pelargonate, etc.), polyoxyalkylene glycol Lumpur, polyphenyl ether, dialkyl diphenyl ether, phosphate ester (tricresyl phosphate, etc.), fluorine-containing compound (perfluoropolyether, fluorinated polyolefin and the like), silicone oils and the like.
Among these base oils, preferred are mineral oil, poly α-olefin, polyol ester, and polyoxyalkylene glycol.
As the base oil of the lubricating oil composition for paper machine of the present invention, the above base oils may be used alone or in combination of two or more.

The kinematic viscosity of these base oils is not particularly limited and is arbitrary, but the lower limit value of the 40 ° C. kinematic viscosity is 10 mm ² / s or more, preferably 20 mm ² / s or more, from the viewpoint of suppressing oil film degradation. preferably 40 mm ² / s or more, and most preferably at 60 mm ² / s or more, the upper limit value, 10000 mm ² / s or less from the viewpoint of friction loss due to agitation resistance is small, preferably not more than 5000 mm ² / s, more preferably 1000 mm ² / s or less. The viscosity index is also arbitrary, but the lower limit is 80 or more, preferably 90 or more, from the viewpoint of suppressing oil film deterioration at high temperatures. In general, the value is 500 or less. Furthermore, although the pour point is also arbitrary, the pour point is usually preferably −5 ° C. or less, more preferably −15 ° C. or less from the viewpoint of low temperature characteristics.

In the lubricating oil composition for paper machine of the present invention, (A) a phosphorus-containing carboxylic acid compound, (B) phosphorothionate, or both of these are blended with the above base oil.
(A) component:
Next, (A) phosphorus-containing carboxylic acid compound will be described.
(A) The phosphorus-containing carboxylic acid compound is not particularly limited as long as it contains both a carboxyl group and a phosphorus atom in the same molecule. However, phosphorylated carboxylic acids are preferred from the viewpoint of extreme pressure and thermal / oxidative stability.

  Examples of the phosphorylated carboxylic acid include a compound represented by the following general formula (1).

［式（１）中、Ｒ^１及びＲ^２は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜３０の炭化水素基を示し、Ｒ^３は炭素数１〜２０のアルキレン基を示し、Ｒ^４は水素原子又は炭素数１〜３０の炭化水素基を示し、炭素数Ｘ^１、Ｘ^２、Ｘ^３及びＸ^４は同一でも異なっていてもよく、それぞれ酸素原子又は硫黄原子を示す。］
一般式（１）中、Ｒ^１及びＲ^２はそれぞれ水素原子又は炭素数１〜３０の炭化水素基を表す。炭素数１〜３０の炭化水素基としては、アルキル基、アルケニル基、シクロアルキル基、ビシクロアルキル基、トリシクロアルキル基、アルキルシクロアルキル基、アルキルビシクロアルキル基、アルキルトリシクロアルキル基、シクロアルキルアルキル基、ビシクロアルキルアルキル基、トリシクロアルキルアルキル基、アリール基、アルキルアリール基、アリールアルキル基等が挙げられる。また、Ｒ^１とＲ^２が結合して下記一般式（２）で表される２価の基を形成してもよい。なお、当該２価の基の２個の結合手はそれぞれＸ^１、Ｘ^２と結合するものである。

[In Formula (1), R ¹ and R ² may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms, and R ³ represents an alkylene group having 1 to 20 carbon atoms. , R ⁴ represents a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms, and the carbon numbers X ¹ , X ² , X ³ and X ⁴ may be the same or different and each represents an oxygen atom or a sulfur atom. ]
In General Formula (1), R ¹ and R ² each represent a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms. Examples of the hydrocarbon group having 1 to 30 carbon atoms include an alkyl group, an alkenyl group, a cycloalkyl group, a bicycloalkyl group, a tricycloalkyl group, an alkylcycloalkyl group, an alkylbicycloalkyl group, an alkyltricycloalkyl group, and a cycloalkylalkyl. Group, bicycloalkylalkyl group, tricycloalkylalkyl group, aryl group, alkylaryl group, arylalkyl group and the like. R ¹ and R ² may be bonded to form a divalent group represented by the following general formula (2). The two bonds of the divalent group are bonded to X ¹ and X ² , respectively.

［式（２）中、Ｒ^５及びＲ^６は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜４のアルキル基を示し、Ｒ^５及びＲ^６の双方がメチル基であることが好ましい。］
Ｒ^１及びＲ^２としては、これらの中でもアルキル基、シクロアルキル基、シクロアルキルアルキル基、トリシクロアルキルアルキル基、アリール基、アルキルアリール基、Ｒ^１とＲ^２とが結合した上記一般式（２）で表されるような２価の基であることが好ましく、アルキル基であることがより好ましい。

[In Formula (2), R ⁵ and R ⁶ may be the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and both R ⁵ and R ⁶ are methyl groups. preferable. ]
Among these, as R ¹ and R ² , among them, an alkyl group, a cycloalkyl group, a cycloalkylalkyl group, a tricycloalkylalkyl group, an aryl group, an alkylaryl group, and the above general formula (2) in which R ¹ and R ² are bonded together ) Is preferably a divalent group, and more preferably an alkyl group.

The alkyl group as R ¹ and R ² may be linear or branched. The alkyl group preferably has 1 to 18 carbon atoms. Specific examples of such an alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tertiary butyl group, a pentyl group, an isopentyl group, a hexyl group, and a heptyl group. 3-heptyl group, octyl group, 2-ethylhexyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, 2-ethylbutyl group, 1 -Methylphenyl group, 1,3-dimethylbutyl group, 1,1,3,3-tetramethylbutyl group, 1-methylhexyl group, isoheptyl group, 1-methylheptyl group, 1,1,3-trimethylhexyl group And 1-methylundecyl group. Among these, a C3-C18 alkyl group is preferable and a C3-C8 alkyl group is more preferable.

Examples of the cycloalkyl group as R ¹ and R ² include a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, and a cyclododecyl group. Among these, a cycloalkyl group having 5 or 6 carbon atoms (cyclopentyl group and cyclohexyl group) is preferable, and a cyclohexyl group is particularly preferable.

The cycloalkylalkyl group as R ¹ and R ² is preferably a cycloalkylmethyl group, more preferably a cycloalkylmethyl group having 6 or 7 carbon atoms, and particularly preferably a cyclopentylmethyl group and a cyclohexylmethyl group.

As the bicycloalkylalkyl group as R ¹ and R ² , a bicycloalkylmethyl group is preferable, a bicycloalkylmethyl group having 9 to 11 carbon atoms is more preferable, and a decalinylmethyl group is particularly preferable.

The tricycloalkylalkyl group as R ¹ and R ² is preferably a tricycloalkylmethyl group, more preferably a tricycloalkylmethyl group having 9 to 15 carbon atoms, represented by the following formula (3) or (4). Particularly preferred are the groups

Ｒ^１、Ｒ^２としてのアリール基及びアルキルアリール基としては、フェニル基、トリル基、キシリル基、エチルフェニル基、ビニルフェニル基、メチルフェニル基、ジメチルフェニル基、トリメチルフェニル基、エチルフェニル基、イソプロピルフェニル基、第三ブチルフェニル基、ジ−第三ブチルフェニル基、２，６−ジ−tert−ブチル−４−メチルフェニル基等が挙げられる。これらの中でも、炭素数６〜１５のアリール基及びアルキルアリール基が好ましい。

Examples of the aryl group and alkylaryl group as R ¹ and R ² include phenyl group, tolyl group, xylyl group, ethylphenyl group, vinylphenyl group, methylphenyl group, dimethylphenyl group, trimethylphenyl group, ethylphenyl group, isopropyl Examples thereof include a phenyl group, a tert-butylphenyl group, a di-tert-butylphenyl group, and a 2,6-di-tert-butyl-4-methylphenyl group. Among these, an aryl group having 6 to 15 carbon atoms and an alkylaryl group are preferable.

R ³ represents an alkylene group having 1 to 20 carbon atoms. Carbon number of this alkylene group becomes like this. Preferably it is 1-10, More preferably, it is 2-6, More preferably, it is 3-4. Moreover, as such an alkylene group, what is represented by following General formula (5) is preferable.

一般式（５）中、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜４の炭化水素基を示し、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０の炭素数の合計は６以下である。また、好ましくは、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜３の炭化水素基を示し、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０の炭素数の合計は５以下である。さらに好ましくは、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１又は２の炭化水素基を示し、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０の炭素数の合計は４以下である。特に好ましくは、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜２の炭化水素基を示し、Ｒ^７、Ｒ^８、Ｒ^９及びＲ^１０の炭素数の合計は３以下である。最も好ましくは、Ｒ^９又はＲ^１０のいずれかがメチル基であり残りの３基が水素原子である。

In the general formula (5), R ⁷ , R ⁸ , R ⁹ and R ¹⁰ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, and R ⁷ , R ⁸ , R The total number of carbon atoms of ⁹ and R ¹⁰ is 6 or less. Preferably, R ⁷ , R ⁸ , R ⁹ and R ¹⁰ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 3 carbon atoms, and R ⁷ , R ⁸ , R ⁹ and The total number of carbon atoms of R ¹⁰ is 5 or less. More preferably, R ⁷ , R ⁸ , R ⁹ and R ¹⁰ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 or 2 carbon atoms, and R ⁷ , R ⁸ , R ⁹ and R 10 The total of ¹⁰ carbon atoms is 4 or less. Particularly preferably, R ⁷ , R ⁸ , R ⁹ and R ¹⁰ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 2 carbon atoms, and R ⁷ , R ⁸ , R ⁹ and R 10 The total of ¹⁰ carbon atoms is 3 or less. Most preferably, either R ⁹ or R ¹⁰ is a methyl group and the remaining three groups are hydrogen atoms.

In general formula (1) ^{R 4} in the show a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms. Examples of the hydrocarbon group include the hydrocarbon groups exemplified in the description of R ¹ and R ² .

Further, X ¹ , X ² , X ³ and X ⁴ in the general formula (1) may be the same or different and each represents an oxygen atom or a sulfur atom. From the point of extreme pressure, one or more of X ¹ , X ² , X ³ or X ⁴ are preferably sulfur atoms, more preferably two or more are sulfur atoms, and two are sulfur atoms. More preferably, the remaining two are oxygen atoms. In this case, it is arbitrary which of X ¹ , X ² , X ³ or X ⁴ is a sulfur atom, but X ¹ and X ² are oxygen atoms, and X ³ and X ⁴ are sulfur atoms. It is preferable.

  As mentioned above, although each group in General formula (1) was demonstrated, since it is excellent in extreme pressure property, (beta) -dithio phosphorylated propionic acid represented by following General formula (6) is used preferably.

［式（６）中、Ｒ^１、Ｒ^２はそれぞれ式（１）中のＲ^１、Ｒ^２と同一の定義内容を示し、Ｒ^７、Ｒ^８、Ｒ^９、Ｒ^１０はそれぞれ（５）中のＲ^７、Ｒ^８、Ｒ^９、Ｒ^１０と同一の定義内容を示す。］
本発明の抄紙機用潤滑油組成物におけるリン含有カルボン酸化合物の含有量は特に制限されないが、組成物全量基準で、好ましくは０．００１〜５質量％、より好ましくは０．００２〜３質量％、さらに好ましくは０．００３〜１質量％である。リン含有カルボン酸化合物の含有量が前記下限値未満では十分な潤滑性が得られない傾向にある。一方、前記上限値を超えても含有量に見合う潤滑性向上効果が得られない傾向にあり、更には熱・酸化安定性や加水分解安定性が低下するおそれがあるので好ましくない。なお、一般式（１）で表されるホスホリル化カルボン酸のうち、Ｒ^４が水素原子である化合物（一般式（６）で表されるβ−ジチオホスホリル化プロピオン酸を含む）の含有量については、好ましくは０．００１〜０．１質量％、より好ましくは０．００２〜０．０８質量％、更に好ましくは０．００３〜０．０７質量％、一層好ましくは０．００４〜０．０６質量％、特に好ましくは０．００５〜０．０５質量％である。当該含有量が０．００１未満の場合は極圧性向上効果が不十分となるおそれがあり、一方、０．１質量％を超えると熱・酸化安定性が低下するおそれがある。

Wherein ^(6), R 1, ^{R 2} represents a ^R 1, ^{R 2} identical definitions and their respective formulas ^{(1), R 7, R 8, R} 9, R 10 are each (5) The same definition content as R ⁷ , R ⁸ , R ⁹ , and R ¹⁰ is shown. ]
The content of the phosphorus-containing carboxylic acid compound in the lubricating oil composition for paper machine of the present invention is not particularly limited, but is preferably 0.001 to 5% by mass, more preferably 0.002 to 3% by mass based on the total amount of the composition. %, More preferably 0.003 to 1% by mass. When the content of the phosphorus-containing carboxylic acid compound is less than the lower limit, sufficient lubricity tends to be not obtained. On the other hand, even if the upper limit is exceeded, there is a tendency that the effect of improving lubricity commensurate with the content tends not to be obtained, and furthermore, heat / oxidation stability and hydrolysis stability may be lowered, which is not preferable. Regarding the phosphorylated carboxylic acid represented by the general formula (1), the content of the compound in which R ⁴ is a hydrogen atom (including β-dithiophosphorylated propionic acid represented by the general formula (6)). Is preferably 0.001 to 0.1% by mass, more preferably 0.002 to 0.08% by mass, still more preferably 0.003 to 0.07% by mass, and still more preferably 0.004 to 0.06%. % By mass, particularly preferably 0.005 to 0.05% by mass. When the content is less than 0.001, the effect of improving extreme pressure may be insufficient. On the other hand, when the content exceeds 0.1% by mass, the heat / oxidation stability may be lowered.

As described above, (A) a phosphorus-containing carboxylic acid compound, (B) phosphorothionate, or both of these are blended with the above base oil in the lubricating oil composition for paper machine of the present invention.
Next, (B) phosphorothioate will be described.

［式中、Ｒ¹¹〜Ｒ¹³は同一でも異なっていてもよく、それぞれ炭素数１〜２４の炭化水素基を示す］
で表される化合物である。 (B) component: phosphorothioate The (B) phosphorothionate according to the present invention has the following general formula (7):

[Wherein R ^{11 to} R ¹³ may be the same or different and each represents a hydrocarbon group having 1 to 24 carbon atoms]
It is a compound represented by these.

Specific examples of the hydrocarbon group having 1 to 24 carbon atoms represented by R ^{11 to} R ¹³ include an alkyl group, a cycloalkyl group, an alkenyl group, an alkylcycloalkyl group, an aryl group, an alkylaryl group, and an arylalkyl group. Etc.

  Examples of the alkyl group include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group. And alkyl groups such as hexadecyl group, heptadecyl group and octadecyl group (these alkyl groups may be linear or branched).

  As a cycloalkyl group, C5-C7 cycloalkyl groups, such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, can be mentioned, for example. Examples of the alkylcycloalkyl group include a methylcyclopentyl group, a dimethylcyclopentyl group, a methylethylcyclopentyl group, a diethylcyclopentyl group, a methylcyclohexyl group, a dimethylcyclohexyl group, a methylethylcyclohexyl group, a diethylcyclohexyl group, a methylcycloheptyl group, Examples thereof include an alkylcycloalkyl group having 6 to 11 carbon atoms such as a dimethylcycloheptyl group, a methylethylcycloheptyl group, and a diethylcycloheptyl group (the substitution position of the alkyl group with the cycloalkyl group is also arbitrary).

  Examples of the alkenyl group include butenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl, octadecenyl Alkenyl groups such as groups (these alkenyl groups may be linear or branched, and the position of the double bond is also optional).

  As an aryl group, aryl groups, such as a phenyl group and a naphthyl group, can be mentioned, for example. Examples of the alkylaryl group include tolyl group, xylyl group, ethylphenyl group, propylphenyl group, butylphenyl group, pentylphenyl group, hexylphenyl group, heptylphenyl group, octylphenyl group, nonylphenyl group, and decylphenyl. Group, an alkylaryl group having 7 to 18 carbon atoms such as undecylphenyl group and dodecylphenyl group (the alkyl group may be linear or branched, and the substitution position on the aryl group is arbitrary). .

  Examples of the arylalkyl group include arylalkyl groups having 7 to 12 carbon atoms such as benzyl group, phenylethyl group, phenylpropyl group, phenylbutyl group, phenylpentyl group, and phenylhexyl group (these alkyl groups may be linear or branched). May be branched).

The hydrocarbon group having 1 to 24 carbon atoms represented by R ^{11 to} R ¹³ is preferably an alkyl group, an aryl group, or an alkylaryl group. An alkylaryl group and a phenyl group are more preferable.

  Specific examples of the phosphorothioate represented by the general formula (7) include tributyl phosphorothioate, tripentyl phosphorothioate, trihexyl phosphorothioate, triheptyl phosphorothioate, and trioctyl. Phosphorothioate, trinonyl phosphorothionate, tridecyl phosphorothionate, triundecyl phosphorothionate, tridodecyl phosphorothionate, tritridecyl phosphorothionate, tritetradecyl phosphorothionate, tri Pentadecyl phosphorothioate, trihexadecyl phosphorothioate, triheptadecyl phosphorothioate, trioctadecyl phosphorothionate, trioleyl phosphorothioate, trif Nyl phosphorothioate, tricresyl phosphorothionate, trixylenyl phosphorothioate, cresyl diphenyl phosphorothionate, xylenyl diphenyl phosphorothionate, tris (n-propylphenyl) phosphorothioate , Tris (isopropylphenyl) phosphothioate, tris (n-butylphenyl) phosphothionate, tris (isobutylphenyl) phosphothionate, tris (s-butylphenyl) phosphothionate, tris (t-butyl) Phenyl) phosphorothioate and the like. Mixtures of these can also be used.

  The content of phosphorothioate is not particularly limited, but the content is usually 0.001 to 10% by mass based on the total amount of lubricating oil composition for paper machine (based on the total amount of base oil and all compounding additives), Preferably it is 0.005-5 mass%, More preferably, it is 0.01-3 mass%.

  In the lubricating oil composition for paper machine of the present invention, the above (A) phosphorus-containing carboxylic acid compound or (B) phosphorothionate may be used alone or both.

Next, optional components other than the essential components will be described below.
(C) component:
Although it is an optional component, it is preferable to add a dispersion type viscosity index improver as the component (C) to the lubricating oil composition for paper machine of the present invention from the viewpoint of sludge suppression.
As the dispersion-type viscosity index improver here, any compound used as a dispersion-type viscosity index improver for lubricating oil can be used. Specifically, for example, the following general formulas (8) and (9 ) Or (10) one or more monomers (C-1) selected from the compounds represented by:
A copolymer obtained by copolymerizing one or more nitrogen-containing monomers (C-2) selected from compounds represented by the following general formula (11) or (12) or a hydride thereof Etc.

(C-1) Component

(C-2) Component

In the general formulas (8), (9) and (10), R ¹⁴ and R ¹⁶ each independently represent a hydrogen atom or a methyl group, R ¹⁵ represents an alkyl group having 1 to 18 carbon atoms, and R ¹⁷ Represents a hydrocarbon group having 1 to 12 carbon atoms, Y ¹ and Y ² are each independently a hydrogen atom, a residue of an alkyl alcohol having 1 to 18 carbon atoms (—OR ²¹ : R ²¹ is a carbon atom having 1 to 18 carbon atoms). Or a residue of a monoalkylamine having 1 to 18 carbon atoms (-NHR ²² : R ²² represents an alkyl group having 1 to 18 carbon atoms).

Specifically, as the alkyl group having 1 to 18 carbon atoms of R ¹⁵ , R ²¹ and R ²² , individually, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, Alkyl groups such as octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group (these alkyl groups may be linear or branched) ) Can be exemplified.

Specific examples of R ¹⁷ include alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl and dodecyl. (These alkyl groups may be linear or branched); butenyl groups, pentenyl groups, hexenyl groups, heptenyl groups, octenyl groups, nonenyl groups, decenyl groups, undecenyl groups, dodecenyl groups and the like (these alkenyl groups) May be linear or branched); a cycloalkyl group having 5 to 7 carbon atoms such as cyclopentyl group, cyclohexyl group, cycloheptyl group; methylcyclopentyl group, dimethylcyclopentyl group, methylethylcyclopentyl group, diethylcyclopentyl group, Methyl cyclohexyl, dimethyl cyclohexyl, methyl ethyl C6-C11 alkylcycloalkyl groups such as cyclohexyl group, diethylcyclohexyl group, methylcycloheptyl group, dimethylcycloheptyl group, methylethylcycloheptyl group, diethylcycloheptyl group (the alkyl group is linear or branched) The bonding position to the cycloalkyl group is also arbitrary); aryl groups such as phenyl group and naphthyl group: tolyl group, xylyl group, ethylphenyl group, propylphenyl group, butylphenyl group, pentylphenyl group, Each alkylaryl group having 7 to 12 carbon atoms such as hexylphenyl group (the alkyl group may be linear or branched, and the bonding position to the aryl group is arbitrary); benzylyl group, phenylethyl group, Phenylpropyl group, phenylbutyl group, phenylpentyl group, phenylhexyl group Arylalkyl group of 7 to 12 carbon atoms such as Le group (the alkyl group may be and straight-chain or branched, also point of attachment to the alkyl group of the aryl group is optional); and the like.

Specific examples of the monomer (C-1) that are preferred include alkyl acrylates having 1 to 18 carbon atoms, alkyl methacrylates having 1 to 18 carbon atoms, olefins having 2 to 20 carbon atoms, styrene, methylstyrene, and anhydrous maleic acid. Examples thereof include acid esters, maleic anhydride amides and mixtures thereof. Among them, the monomer of the component (C-1) is a monomer represented by the general formula (8), for example, an alkyl (meth) acrylate having an alkyl group having 1 to 18 carbon atoms.
On the other hand, in General Formula (11) and General Formula (12) as the component (C-2), R ¹⁸ and R ²⁰ each independently represent a hydrogen atom or a methyl group, and R ¹⁹ has 2 to 18 carbon atoms. And a represents an integer of 0 or 1.
Y ³ and Y ⁴ each independently represent an organic group containing a nitrogen atom having 1 to 30 carbon atoms.
Y ³ and Y ⁴ are preferably a group having a ring, and such a ring is more preferably a group having an aliphatic ring rather than an aromatic ring.
Y ³ and Y ⁴ are preferably groups having a 6-membered ring from the viewpoint of sludge suppression.
Y ³ and Y ⁴ are more preferably a group having an oxygen-containing atomic ring from the viewpoint of sludge suppression.
Y ³ and Y ⁴ are preferably groups having one nitrogen atom.
Y ³ and Y ⁴ are most preferably a morpholino group from the viewpoint of sludge suppression.

Specific examples of R ¹⁹ include ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, nonylene, decylene, undecylene, dodecylene, tridecylene, tetradecylene, pentadecylene. And an alkylene group such as a group, hexadecylene group, heptadecylene group, and octadecylene group (these alkylene groups may be linear or branched).

  Among the general formula (11) and general formula (12) as the component (C-2) monomer, the monomer represented by the general formula (11) is preferable from the viewpoint of sludge suppression. Specific examples include dimethylaminomethyl methacrylate, diethylaminomethyl methacrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, 2-methyl-5-vinylpyridine, morpholinomethyl methacrylate, morpholinoethyl methacrylate, and mixtures thereof.

  From the above, the (C) dispersion type viscosity index improver as an optional component means a copolymer having a nitrogen-containing monomer such as the component (C-2) as a comonomer. The dispersion type viscosity index improver which is the optional component (C) is selected from one or more monomers selected from the components (C-1) and the component (C-2). It can be obtained by copolymerizing one or more nitrogen-containing monomers. Although the molar ratio of the (C-1) component and the (C-2) component in the copolymerization is arbitrary, it is generally about 80:20 to 95: 5. Although the reaction method of copolymerization is arbitrary, it is usually easy to carry out copolymerization by subjecting the (C-1) component and the (C-2) component to radical solution polymerization in the presence of a polymerization initiator such as benzoyl peroxide. Coalescence is obtained. The number average molecular weight of the dispersion type viscosity index improver of the component (C) is also arbitrary, but usually the number average molecular weight is 1,000 to 1,500,000, preferably 10,000 to 200,000. It is desirable to use

  The upper limit of the content of the component (C) as an optional component in the lubricating oil composition for paper machine of the present invention is 10% by mass, preferably 5% by mass, more preferably 2% by mass based on the total amount of the composition. is there. Even if the content exceeds 10% by mass, no further improvement in the effect of inhibiting sludge formation corresponding to the content is observed, and the viscosity is lowered by shearing, which is not preferable. On the other hand, the lower limit of the content of component (C) is 0.01% by mass, preferably 0.05% by mass, and more preferably 0.1% by mass, based on the total amount of the composition. When the content of the component (C) is less than 0.01% by mass, the effect of addition is not observed, and the sludge generation suppressing effect of the lubricating oil composition for paper machine may be deteriorated, which is not preferable.

(D) component:
Although it is an optional component, in order to improve the friction characteristics, the lubricating oil composition for paper machine of the present invention contains at least one compound represented by the following general formulas (13) to (15) as the component (D). It is preferable.
^{R 23 -CO-NR 24 - (} CH 2) n -COOX 5 (13)
(In the formula, R ²³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ²⁴ is an alkyl group having 1 to 4 carbon atoms, X ⁵ is hydrogen, and an alkyl group having 1 to 30 carbon atoms. Or an alkenyl group having 1 to 30 carbon atoms, and n represents an integer of 1 to 4.)
[R ²³ —CO—NR ²⁴ — (CH ₂ ) _n —COO] _m Y ⁵ (14)
(Wherein R ²³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ²⁴ is an alkyl group having 1 to 4 carbon atoms, Y ⁵ is an alkali metal or alkaline earth metal, and n is (An integer of 1 to 4, m represents 1 when Y is an alkali metal, and 2 when Y is an alkaline earth metal.)
^{[R 23 -CO-NR 24 -} (CH 2) n -COO] m -Z- (OH) m '(15)
(Wherein R ²³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ²⁴ is an alkyl group having 1 to 4 carbon atoms, and Z is a hydroxyl group of a polyhydric alcohol having 2 or more valences) And m represents an integer of 1 or more, m ′ represents an integer of 0 or more, m + m ′ represents a valence of Z, and n represents an integer of 1 to 4.)

In general formulas (13) to (15), R ²³ represents an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms. From the viewpoint of solubility in base oil, the alkyl group or alkenyl group must have 6 or more carbon atoms, preferably 7 or more carbon atoms, and more preferably 8 or more carbon atoms. Further, from the viewpoint of storage stability and the like, it is necessary that the alkyl group or alkenyl group has 30 or less carbon atoms, preferably 24 or less carbon atoms, and more preferably 20 or less carbon atoms. Specific examples of such alkyl groups and alkenyl groups include hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, Alkyl groups such as heptadecyl group, octadecyl group, nonadecyl group, icosyl group (these alkyl groups may be linear or branched); hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group, undecenyl group, dodecenyl group Group, tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group, heptadecenyl group, octadecenyl group, nonadecenyl group, icocenyl group, etc. Are also optional)

In general formulas (13) to (15), R ²⁴ represents an alkyl group having 1 to 4 carbon atoms. From the viewpoint of storage stability and the like, the alkyl group is required to be an alkyl group having 4 or less carbon atoms, preferably 3 or less carbon atoms, and more preferably 2 or less carbon atoms. In general formulas (13) to (15), n represents an integer of 1 to 4. From the viewpoint of storage stability and the like, it is necessary to be an integer of 4 or less, preferably 3 or less, and more preferably 2 or less.

In General Formula (13), X ⁵ represents hydrogen, an alkyl group having 1 to 30 carbon atoms, or an alkenyl group having 1 to 30 carbon atoms. The alkyl group or alkenyl group represented by X ⁵ needs to have 30 or less carbon atoms from the viewpoint of storage stability and the like, preferably 20 or less carbon atoms, and more preferably 10 or less carbon atoms. preferable. Specific examples of such an alkyl group or alkenyl group include alkyl groups such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group. (These alkyl groups may be linear or branched); alkenyl groups such as ethenyl group, propenyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group (these alkenyl groups) May be linear or branched, and the position of the double bond is arbitrary. Moreover, it is preferable that it is an alkyl group from points, such as being excellent in sludge resistance. X ⁵ is preferably hydrogen, an alkyl group having 1 to 20 carbon atoms, or an alkenyl group having 1 to 20 carbon atoms from the viewpoint of improving the friction characteristics, improving the durability of the friction characteristic effect, It is more preferably hydrogen or an alkyl group having 1 to 20 carbon atoms, and even more preferably hydrogen or an alkyl group having 1 to 10 carbon atoms.

In the general formula (14), Y ⁵ represents an alkali metal or an alkaline earth metal, and specific examples include sodium, potassium, magnesium, calcium and the like. Among these, alkaline earth metals are preferable from the viewpoint of improving the sustainability of the friction characteristic effect. In the general formula (14), m represents 1 when Y ⁵ is an alkali metal, and 2 when Y is an alkaline earth metal.

  In general formula (15), Z represents the residue except the hydroxyl group of the polyhydric alcohol more than bivalence. Specific examples of such polyhydric alcohols include ethylene glycol, propylene glycol, 1,4-butanediol, 1,2-butanediol, neopentyl glycol, 1,6-hexanediol, 1,2- Octanediol, 1,8-octanediol, isoprene glycol, 3-methyl-1,5-pentanediol, sorbite, catechol, resorcin, hydroquinone, bisphenol A, bisphenol F, hydrogenated bisphenol A, hydrogenated bisphenol F, dimer diol Divalent alcohols such as glycerin, 2- (hydroxymethyl) -1,3-propanediol, 1,2,3-butanetriol, 1,2,3-pentanetriol, 2-methyl-1,2,3 -Propanetriol, 2-methyl-2,3,4- Tantriol, 2-ethyl-1,2,3-butanetriol, 2,3,4-pentanetriol, 2,3,4-hexanetriol, 4-propyl-3,4,5-heptanetriol, 2,4 -Trihydric alcohols such as dimethyl-2,3,4-pentanetriol, 1,2,4-butanetriol, 1,2,4-pentanetriol, trimethylolethane, trimethylolpropane; pentaerythritol, erythritol, 1, 2,3,4-pentanetetrol, 2,3,4,5-hexanetetrol, 1,2,4,5-pentanetetrol, 1,3,4,5-hexanetetrol, diglycerin, sorbitan Tetrahydric alcohols such as adonitol, arabitol, xylitol, triglycerin, etc .; dipentaerythritol Le, sorbitol, mannitol, iditol, inositol, dulcitol, talose, hexavalent alcohols such as allose, polyglycerin or their dehydrated condensates and the like.

  In the general formula (15), m is an integer of 1 or more, m ′ is an integer of 0 or more, and m + m ′ is the same as the valence of Z. That is, all of the hydroxyl groups of the polyhydric alcohol of Z may be substituted, or only a part thereof may be substituted.

The component (D) as an optional component is at least one compound selected from the general formulas (13) to (15). From the viewpoint of improving the durability of the friction characteristic effect, the general formula ( It is preferably at least one compound selected from 13) and (14). Further, only one compound selected from the general formulas (13) to (15) may be used alone, or a mixture of two or more compounds may be used.
As a preferable example of the compound represented by the general formula (13), N-oleoyl sarcosine in which R ²³ is an alkenyl group having 17 carbon atoms, R ²⁴ is a methyl group, X ⁵ is hydrogen, and n is 1 is used. Can be mentioned.

  The upper limit of the content of the optional component (D) in the lubricating oil composition for paper machine of the present invention is 5% by mass, preferably 2% by mass, more preferably 1% by mass based on the total amount of the composition. When the content exceeds 5% by mass, further improvement in friction characteristics corresponding to the content is not observed, and storage stability is lowered, which is not preferable. On the other hand, the lower limit of the content of the component (D) is 0.001% by mass, preferably 0.003% by mass, and more preferably 0.005% by mass based on the total amount of the composition. When the content of the component (D) is less than 0.001% by mass, the effect of improving the friction characteristics is not seen, which is not preferable.

(E) component:
The lubricating oil composition for paper machine of the present invention is an optional component, but from the viewpoint of further improving the frictional properties, as a component (E), (E) a compound represented by the following general formula (16) is used. It is preferable to contain.
R ²⁵ —CH ₂ COOH Formula (16)
(In the formula, R ²⁵ represents an alkyl group having 7 to 29 carbon atoms, an alkenyl group having 7 to 29 carbon atoms, or a group represented by the general formula (17).)
R ²⁶ —C ₆ H ₄ O— (17)
(In the formula, R ²⁶ represents an alkyl group having 1 to 20 carbon atoms or hydrogen.)

In general formula (16), R ²⁵ represents an alkyl group having 7 to 29 carbon atoms, an alkenyl group having 7 to 29 carbon atoms, or a group represented by general formula (17). The alkyl group represented by R ²⁵ needs to have 7 to 29 carbon atoms. In view of solubility in the base oil, it is necessary that the number of carbon atoms is 7 or more, and it is preferable that the number of carbon atoms is 9 or more. Further, from the viewpoint of storage stability and the like, it is necessary to have 29 or less carbon atoms, preferably 22 or less carbon atoms, and more preferably 19 or less carbon atoms. Specific examples of such alkyl groups include heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, Nonadecyl group and the like (these alkyl groups may be linear or branched).

The alkenyl group represented by R ²⁵ needs to have 7 to 29 carbon atoms. In view of solubility in the base oil, it is necessary that the number of carbon atoms is 7 or more, and it is preferable that the number of carbon atoms is 9 or more. Further, from the viewpoint of storage stability and the like, it is necessary to have 29 or less carbon atoms, preferably 22 or less carbon atoms, and more preferably 19 or less carbon atoms. Specific examples of such alkenyl groups include heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl, octadecenyl, A nonadecenyl group and the like (these alkenyl groups may be linear or branched).

In general formula (17), R ²⁶ represents an alkyl group having 1 to 20 carbon atoms or hydrogen. The alkyl group represented by R ²⁶ needs to have 20 or less carbon atoms from the viewpoint of storage stability and the like, preferably 19 or less carbon atoms, and more preferably 15 or less carbon atoms. Moreover, it is preferable that it is C3 or more from points, such as the solubility to base oil, and it is more preferable that it is C5 or more. In the case where R ²⁶ is an alkyl group, the substitution position is arbitrary, but the para-position or the meta-position is preferable, and the para-position is more preferable from the viewpoint of excellent frictional properties. In the general formula (16), R ²⁵ is represented by the general formula (17) regardless of whether it is an alkyl group having 7 to 29 carbon atoms or an alkenyl group having 7 to 29 carbon atoms, as described above. Although it may be a group, it is preferably a group represented by the general formula (17) from the viewpoint of superior friction characteristics.

  In the oil composition of the present invention, the content when the component (E) is blended is arbitrary, but if blended in a large amount, the sludge resistance may be lowered, so that it is 5% by mass or less based on the total amount of the composition. It is preferable that it is 1 mass% or less, and it is still more preferable that it is 0.5 mass% or less. On the other hand, it is preferably 0.001% by mass or more, more preferably 0.003% by mass or more, more preferably 0.005% by mass or more based on the total amount of the composition from the viewpoint of sufficiently exerting the effect of improving the friction characteristics. Even more preferably, it is at least mass%.

(F) component:
In the lubricating oil composition for a paper machine of the present invention, it is preferable to use a sulfur-based extreme pressure agent as an optional component (F) from the viewpoint of improving extreme pressure.
Specific examples of the sulfur-based extreme pressure agent include sulfurized fats and oils, sulfurized fatty acids, sulfurized esters, sulfurized olefins, dihydrocarbyl (poly) sulfide, thiadiazole compounds, alkylthiocarbamoyl compounds, thiocarbamate compounds, thioterpene compounds, dialkylthiodipropionates. Examples thereof include compounds, sulfide mineral oil, zinc dithiophosphate compounds, zinc dithiocarbamate compounds, molybdenum dithiophosphates and molybdenum dithiocarbamates. These sulfur type extreme pressure agents may be used individually by 1 type, and may be used as a 2 or more types of mixture.

  Sulfurized fats and oils are obtained by reacting sulfur and sulfur-containing compounds with fats and oils (lard oil, whale oil, vegetable oil, fish oil, etc.), and the sulfur content is not particularly limited, but is generally 5 to 30% by mass. Those are preferred. Specific examples thereof include sulfurized lard, sulfurized rapeseed oil, sulfurized castor oil, sulfurized soybean oil, sulfurized rice bran oil, and mixtures thereof.

  Examples of sulfurized fatty acids include sulfurized oleic acid, and examples of sulfurized esters include reaction of unsaturated fatty acids (including oleic acid, linoleic acid, or fatty acids extracted from the above-mentioned animal and vegetable oils) and various alcohols. And the like obtained by sulfiding the unsaturated fatty acid ester obtained by mixing with an arbitrary method, specifically, for example, methyl sulfide oleate, sulfurized rice bran fatty acid octyl, and a mixture thereof. Can be mentioned.

Examples of the sulfurized olefin include a compound represented by the following general formula (18).
This compound is obtained by reacting an olefin having 2 to 15 carbon atoms or a dimer to tetramer thereof with a sulfurizing agent such as sulfur or sulfur chloride. As the olefin, propylene, isobutene, diisobutene and the like are preferable.

_{^{R 27 -S a -R 28 (18}} )
[Wherein, R ²⁷ represents an alkenyl group having 2 to 15 carbon atoms, R ²⁸ represents an alkyl group or alkenyl group having 2 to 15 carbon atoms, and a represents an integer of 1 to 8. ]
Dihydrocarbyl (poly) sulfide is a compound represented by the following general formula (19). Here, when R ²⁹ and R ³⁰ are alkyl groups, they may be referred to as alkyl sulfides.

R ²⁹ -S _b -R ³⁰ (19)
[In the formula, R ²⁹ and R ³⁰ may be the same or different and each represents a chain alkyl group having 1 to 20 carbon atoms, a branched or cyclic alkyl group, an aryl group having 6 to 20 carbon atoms, or 7 carbon atoms. Represents an alkylaryl group of -20 or an arylalkyl group of 7-20 carbon atoms, and b represents an integer of 1-8. ]
Specific examples of R ²⁹ and R ³⁰ in the general formula (19) include n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, straight chain or Branched pentyl group, linear or branched hexyl group, linear or branched heptyl group, linear or branched octyl group, linear or branched nonyl group, linear or branched decyl group, linear or branched Undecyl group, linear or branched dodecyl group, linear or branched tridecyl group, linear or branched tetradecyl group, linear or branched pentadecyl group, linear or branched hexadecyl group, linear or branched heptadecyl group A linear or branched alkyl group such as a linear or branched octadecyl group, a linear or branched nonadecyl group, a linear or branched icosyl group; an aryl group such as a phenyl group or a naphthyl group; a tolyl group ( All structural isomers Including), ethylphenyl group (including all structural isomers), linear or branched propylphenyl group (including all structural isomers), linear or branched butylphenyl group (including all structural isomers) ), Straight chain or branched pentylphenyl group (including all structural isomers), straight chain or branched hexylphenyl group (including all structural isomers), straight chain or branched heptylphenyl group (all structures) Isomers), linear or branched octylphenyl groups (including all structural isomers), linear or branched nonylphenyl groups (including all structural isomers), linear or branched decylphenyl groups (Including all structural isomers), linear or branched undecylphenyl group (including all structural isomers), linear or branched dodecylphenyl group (including all structural isomers), xylyl group (including all structural isomers) Including all structural isomers), Ethylmethylphenyl group (including all structural isomers), diethylphenyl group (including all structural isomers), di (straight or branched) propylphenyl group (including all structural isomers), di ( Linear or branched) butylphenyl group (including all structural isomers), methyl naphthyl group (including all structural isomers), ethyl naphthyl group (including all structural isomers), linear or branched Propyl naphthyl group (including all structural isomers), linear or branched butyl naphthyl group (including all structural isomers), dimethyl naphthyl group (including all structural isomers), ethyl methyl naphthyl group (all ), Diethyl naphthyl group (including all structural isomers), di (linear or branched) propyl naphthyl group (including all structural isomers), di (linear or branched) Butylnaphthyl group ( Alkylaryl groups such as all structural isomers; arylalkyl groups such as benzyl, phenylethyl groups (including all isomers), phenylpropyl groups (including all isomers), etc. Can do. Among these, ^{R 29} and ^{R 30} in the general formula (19), propylene, 1-butene or an alkyl group has been 3 to 18 carbon atoms derived from isobutylene, or an aryl group having a carbon number of 6-8, alkyl An aryl group or an arylalkyl group is preferable. Examples of these groups include isopropyl group, branched hexyl group derived from propylene dimer (including all branched isomers), and propylene trimer. Branched nonyl groups derived from the body (including all branched isomers), branched dodecyl groups derived from the propylene tetramer (including all branched isomers), 5 quantities of propylene Branched pentadecyl groups derived from the body (including all branched isomers), branched octadecyl groups derived from the propylene hexamer (including all branched isomers), ec-butyl group, tert-butyl group, branched octyl group derived from 1-butene dimer (including all branched isomers), branched octyl group derived from isobutylene dimer (Including all branched isomers), branched dodecyl group derived from 1-butene trimer (including all branched isomers), branched derived from isobutylene trimer Dodecyl group (including all branched isomers), branched hexadecyl group (including all branched isomers) derived from 1-butene tetramer, fraction derived from isobutylene tetramer Alkyl groups such as branched hexadecyl groups (including all branched isomers); phenyl groups, tolyl groups (including all structural isomers), ethylphenyl groups (including all structural isomers), xylyl groups Alkyl compounds such as (including all structural isomers) Examples include a reel group; an arylalkyl group such as a benzyl group and a phenylethyl group (including all isomers).

Furthermore, R ²⁹ and R ³⁰ in the general formula (19) are each independently a branched alkyl group having 3 to 18 carbon atoms derived from ethylene or propylene from the viewpoint of improving the processing efficiency and tool life. It is more preferable that it is a branched alkyl group having 6 to 15 carbon atoms derived from ethylene or propylene.

  Examples of the dihydrocarbyl (poly) sulfide represented by the general formula (19) include dibenzyl polysulfide, various dinonyl polysulfides, various didodecyl polysulfides, various dibutyl polysulfides, various dioctyl polysulfides, diphenyl polysulfide, dicyclohexyl polysulfide, and these. A mixture etc. can be mentioned preferably.

  Examples of the thiadiazole compound include 1,3,4-thiadiazole represented by the following general formula (20), 1,2,4-thiadiazole compound represented by the following general formula (21), and the following general formula (22). The 1,4,5-thiadiazole compound represented by these is mentioned.

［式中、Ｒ^３１及びＲ^３２は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜２０の炭化水素基を示し、ｃ及びｄは同一でも異なっていてもよく、それぞれ０〜８の整数を示す］

[Wherein, R ³¹ and R ³² may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms; c and d may be the same or different; Indicates an integer]

  Specific examples of such thiadiazole compounds include 2,5-bis (n-hexyldithio) -1,3,4-thiadiazole, 2,5-bis (n-octyldithio) -1,3,4-thiadiazole. 2,5-bis (n-nonyldithio) -1,3,4-thiadiazole, 2,5-bis (1,1,3,3-tetramethylbutyldithio) -1,3,4-thiadiazole, 3, 5-bis (n-hexyldithio) -1,2,4-thiadiazole, 3,5-bis (n-octyldithio) -1,2,4-thiadiazole, 3,5-bis (n-nonyldithio) -1 , 2,4-thiadiazole, 3,5-bis (1,1,3,3-tetramethylbutyldithio) -1,2,4-thiadiazole, 4,5-bis (n-hexyldithio) -1,2 , 3-thiadiazole, 4 5-bis (n-octyldithio) -1,2,3-thiadiazole, 4,5-bis (n-nonyldithio) -1,2,3-thiadiazole, 4,5-bis (1,1,3,3) Preferred examples include -tetramethylbutyldithio) -1,2,3-thiadiazole and a mixture thereof.

  Examples of the alkylthiocarbamoyl compound include compounds represented by the following general formula (23).

［式中、Ｒ^３３〜Ｒ^３６は同一でも異なっていてもよく、それぞれ炭素数１〜２０のアルキル基を示し、ｅは１〜８の整数を示す。］
このようなアルキルチオカルバモイル化合物の具体例としては、ビス（ジメチルチオカルバモイル）モノスルフィド、ビス（ジブチルチオカルバモイル）モノスルフィド、ビス（ジメチルチオカルバモイル）ジスルフィド、ビス（ジブチルチオカルバモイル）ジスルフィド、ビス（ジアミルチオカルバモイル）ジスルフィド、ビス（ジオクチルチオカルバモイル）ジスルフィドおよびこれらの混合物などを好ましく挙げることができる。

[Wherein, R ^{33 to} R ³⁶ may be the same or different and each represents an alkyl group having 1 to 20 carbon atoms, and e represents an integer of 1 to 8. ]
Specific examples of such alkylthiocarbamoyl compounds include bis (dimethylthiocarbamoyl) monosulfide, bis (dibutylthiocarbamoyl) monosulfide, bis (dimethylthiocarbamoyl) disulfide, bis (dibutylthiocarbamoyl) disulfide, and bis (diamil). Preferred examples include thiocarbamoyl) disulfide, bis (dioctylthiocarbamoyl) disulfide, and mixtures thereof.

  Examples of the alkylthiocarbamate compound include a compound represented by the following general formula (24).

［式中、Ｒ^３７〜Ｒ^４０は同一でも異なっていてもよく、それぞれ炭素数１〜２０のアルキル基を示し、Ｒ^４１は炭素数１〜１０のアルキル基を示す。］
このようなアルキルチオカーバメート化合物の具体例としては、メチレンビス（ジブチルジチオカーバメート）、メチレンビス［ジ（２−エチルヘキシル）ジチオカーバメート］などを好ましく挙げることができる。

[Wherein, R ^{37 to} R ⁴⁰ may be the same or different and each represents an alkyl group having 1 to 20 carbon atoms, and R ⁴¹ represents an alkyl group having 1 to 10 carbon atoms. ]
Preferable examples of such alkylthiocarbamate compounds include methylenebis (dibutyldithiocarbamate), methylenebis [di (2-ethylhexyl) dithiocarbamate] and the like.

  Further, examples of the thioterpene compound include a reaction product of phosphorus pentasulfide and pinene, and examples of the dialkylthiodipropionate compound include dilauryl thiodipropionate, distearyl thiodipropionate, and a mixture thereof. be able to.

  Sulfided mineral oil refers to one obtained by dissolving elemental sulfur in mineral oil. Here, the mineral oil used in the sulfide mineral oil according to the present invention is not particularly limited. Specifically, specifically, a lubricating oil fraction obtained by subjecting crude oil to atmospheric distillation and vacuum distillation is used as a solvent. Examples thereof include paraffinic mineral oil, naphthenic mineral oil, and the like, which are refined by appropriately combining purification treatments such as deblocking, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid washing, and clay treatment. In addition, as the elemental sulfur, any form such as a lump, powder, molten liquid, etc. may be used, but when powdered or molten liquid elemental sulfur is used, it is efficiently dissolved in the base oil. Is preferable. In addition, molten liquid elemental sulfur has the advantage that the melting operation can be performed in a very short time because the liquids are mixed together, but it must be handled above the melting point of elemental sulfur, heating equipment, etc. It is not always easy to handle because it requires special equipment and is handled in a high temperature atmosphere. On the other hand, powdery simple sulfur is particularly preferable because it is inexpensive and easy to handle, and the time required for dissolution is sufficiently short. Moreover, although there is no restriction | limiting in particular in the sulfur content in the sulfide mineral oil concerning this invention, Preferably it is 0.05-1.0 mass% normally on the basis of the sulfide mineral oil whole quantity, More preferably, it is 0.1-0. 5% by mass.

The zinc dithiophosphate compound, the zinc dithiocarbamate compound, the molybdenum dithiophosphate and the molybdenum dithiocarbamate are respectively represented by the following general formulas (25) to (28).
:

Expression (25) in ^{~ (28), R 42,} R 43, R 44, R 45, R 46, R 47, R 48, R 49, R 50, R 51, R 52, R 53, R 54, R ⁵⁵ , R ⁵⁶ and R ⁵⁷ may be the same or different and each represents a hydrocarbon group having 1 or more carbon atoms, and X ⁶ and X ⁷ each represents an oxygen atom or a sulfur atom]
The compound represented by these is meant.

^{Wherein, R 42, R 43, R} 44, R 45, R 46, R 47, R 48, R 49, R 50, R 51, R 52, R 53, R 54, R 55, R 56 and ^{R 57} Specific examples of the hydrocarbon group represented by: methyl group, ethyl group, propyl group (including all branched isomers), butyl group (including all branched isomers), pentyl group (including Including all branched isomers), hexyl group (including all branched isomers), heptyl group (including all branched isomers), octyl group (including all branched isomers), nonyl Groups (including all branched isomers), decyl groups (including all branched isomers), undecyl groups (including all branched isomers), dodecyl groups (including all branched isomers) , Tridecyl group (including all branched isomers), tetradecyl Groups (including all branched isomers), pentadecyl groups (including all branched isomers), hexadecyl groups (including all branched isomers), heptadecyl groups (including all branched isomers) , Octadecyl group (including all branched isomers), nonadecyl group (including all branched isomers), icosyl group (including all branched isomers), heicosyl group (including all branched isomers) Alkyl groups such as docosyl group (including all branched isomers), tricosyl group (including all branched isomers), tetracosyl group (including all branched isomers); cyclopentyl group, cyclohexyl Group, cycloalkyl group such as cycloheptyl group; methylcyclopentyl group (including all substituted isomers), ethylcyclopentyl group (including all substituted isomers), dimethyl Clopentyl group (including all substituted isomers), propylcyclopentyl group (including all branched isomers, including substituted isomers), methylethylcyclopentyl group (including all substituted isomers), trimethylcyclopentyl group (including all substituted isomers) Substituted isomers), butylcyclopentyl group (all branched isomers, including substituted isomers), methylpropylcyclopentyl group (including all branched isomers, substituted isomers), diethylcyclopentyl group (all Substituted isomers), dimethylethylcyclopentyl group (including all substituted isomers), methylcyclohexyl group (including all substituted isomers), ethylcyclohexyl group (including all substituted isomers), dimethylcyclohexyl group (Including all substituted isomers), propylcyclohexyl groups (all Branched isomers, including substituted isomers, methylethylcyclohexyl group (including all substituted isomers), trimethylcyclohexyl group (including all substituted isomers), butylcyclohexyl group (all branched isomers, Substituted isomers), methylpropylcyclohexyl group (including all branched isomers, including substituted isomers), diethylcyclohexyl group (including all substituted isomers), dimethylethylcyclohexyl group (including all substituted isomers) ), Methylcycloheptyl group (including all substituted isomers), ethylcycloheptyl group (including all substituted isomers), dimethylcycloheptyl group (including all substituted isomers), propylcycloheptyl group (including All branched isomers, including substituted isomers), methylethylcycloheptyl group (all substituted isomers) ), Trimethylcycloheptyl group (including all substituted isomers), butylcycloheptyl group (including all branched isomers, including substituted isomers), methylpropylcycloheptyl group (including all branched isomers), Substituted isomers), diethylcycloheptyl group (including all substituted isomers), dimethylethylcycloheptyl group (including all substituted isomers) and other alkyl cycloalkyl groups; phenyl group, naphthyl group and other aryls Group; tolyl group (including all substituted isomers), xylyl group (including all substituted isomers), ethylphenyl group (including all substituted isomers), propylphenyl group (all branched isomers, Substituted isomers), methylethylphenyl group (including all substituted isomers), trimethylphenyl group (including all substituted isomers) ), Butylphenyl group (including all branched and substituted isomers), methylpropylphenyl group (including all branched and substituted isomers), and diethylphenyl group (including all substituted isomers) Dimethylethylphenyl group (including all substituted isomers), pentylphenyl group (including all branched isomers, including substituted isomers), hexylphenyl group (including all branched isomers, substituted isomers) ), Heptylphenyl group (including all branched isomers, substituted isomers), octylphenyl group (including all branched isomers, substituted isomers), nonylphenyl group (all branched isomers, Including substituted isomers), decylphenyl group (including all branched isomers and substituted isomers), undecylphenyl group (including all branched and substituted isomers), dodecylphenyl Group (including all branched isomers, substituted isomers), tridecylphenyl group (including all branched isomers, substituted isomers), tetradecylphenyl group (all branched isomers, substituted isomers) ), Pentadecylphenyl group (including all branched and substituted isomers), hexadecylphenyl group (including all branched and substituted isomers), heptadecylphenyl group (including all branched isomers) Alkylaryl groups such as branched isomers, including substituted isomers, octadecylphenyl groups (including all branched isomers and substituted isomers); benzyl groups, phenethyl groups, phenylpropyl groups (all branched isomers) And arylalkyl groups such as phenylbutyl group (including all branched isomers).

  In the lubricating oil composition for a paper machine of the present invention, the content of the sulfur-based extreme pressure agent as the component (F) is arbitrary, but from the viewpoint of improving the extreme pressure of the lubricating oil composition for the paper machine to be obtained, the composition The lower limit is preferably 0.01% by mass or more, more preferably 0.05% by mass or more, and even more preferably 0.1% by mass or more, based on the total amount of products. In addition, from the point that the effect of commensurate with the addition amount is not obtained even if blended more than that, the upper limit value of the content of the sulfur extreme pressure agent is preferably 10% by mass or less based on the total amount of the composition, It is more preferably 5% by mass or less, still more preferably 3% by mass or less, and most preferably 1% by mass or less.

(G) component:
In the lubricating oil composition for a paper machine of the present invention, an epoxy compound can be blended as the component (G), although it is an optional component from the viewpoint of sludge suppression. The following are mentioned as an epoxy compound.
(1) Phenyl glycidyl ether type epoxy compound (2) Alkyl glycidyl ether type epoxy compound (3) Glycidyl ester type epoxy compound (4) Allyl oxirane compound (5) Alkyl oxirane compound (6) Alicyclic epoxy compound (7) Epoxy Fatty acid monoester (8) epoxidized vegetable oil

  (1) Specific examples of the phenyl glycidyl ether type epoxy compound include phenyl glycidyl ether and alkylphenyl glycidyl ether. As used herein, the alkylphenyl glycidyl ether includes those having 1 to 3 alkyl groups having 1 to 13 carbon atoms, and those having one alkyl group having 4 to 10 carbon atoms, such as n-butylphenyl glycidyl. Ether, i-butylphenyl glycidyl ether, sec-butylphenyl glycidyl ether, tert-butylphenyl glycidyl ether, pentylphenyl glycidyl ether, hexylphenyl glycidyl ether, heptylphenyl glycidyl ether, octylphenyl glycidyl ether, nonylphenyl glycidyl ether, decylphenyl A glycidyl ether etc. can be illustrated as a preferable thing.

  (2) Specific examples of the alkyl glycidyl ether type epoxy compound include decyl glycidyl ether, undecyl glycidyl ether, dodecyl glycidyl ether, tridecyl glycidyl ether, tetradecyl glycidyl ether, 2-ethylhexyl glycidyl ether, neopentyl glycol di Examples thereof include glycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, 1,6-hexanediol diglycidyl ether, sorbitol polyglycidyl ether, polyalkylene glycol monoglycidyl ether, polyalkylene glycol diglycidyl ether and the like.

(3) As a glycidyl ester type epoxy compound, specifically, the following general formula (29):

[Wherein R ⁵⁸ represents a hydrocarbon group having 1 to 18 carbon atoms]
The compound represented by these is mentioned.

In the above formula (29), R ⁵⁸ represents a hydrocarbon group having 1 to 18 carbon atoms. Examples of such a hydrocarbon group include an alkyl group having 1 to 18 carbon atoms, an alkenyl group having 2 to 18 carbon atoms, C5-C7 cycloalkyl group, C6-C18 alkylcycloalkyl group, C6-C10 aryl group, C7-C18 alkylaryl group, C7-C18 arylalkyl group, etc. Is mentioned. Among these, an alkylphenyl group having an alkyl group having 5 to 15 carbon atoms, an alkenyl group having 2 to 15 carbon atoms, a phenyl group, and an alkyl group having 1 to 4 carbon atoms is preferable.

  Among the glycidyl ester type epoxy compounds, preferred examples include glycidyl-2,2-dimethyloctanoate, glycidyl benzoate, glycidyl-tert-butyl benzoate, glycidyl acrylate, glycidyl methacrylate, and the like.

  (4) Specific examples of the allyloxirane compound include 1,2-epoxystyrene, alkyl-1,2-epoxystyrene, and the like.

  (5) Specific examples of the alkyloxirane compound include 1,2-epoxybutane, 1,2-epoxypentane, 1,2-epoxyhexane, 1,2-epoxyheptane, 1,2-epoxyoctane, 1 , 2-epoxynonane, 1,2-epoxydecane, 1,2-epoxyundecane, 1,2-epoxydodecane, 1,2-epoxytridecane, 1,2-epoxytetradecane, 1,2-epoxypentadecane, 1, 2,2-epoxyhexadecane, 1,2-epoxyheptadecane, 1,1,2-epoxyoctadecane, 2-epoxynonadecane, 1,2-epoxyicosane and the like.

(6) As an alicyclic epoxy compound, the following general formula (30):

And a compound in which the carbon atom constituting the epoxy group directly constitutes an alicyclic ring.

  Specific examples of the alicyclic epoxy compound include 1,2-epoxycyclohexane, 1,2-epoxycyclopentane, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, and bis (3,4 -Epoxycyclohexylmethyl) adipate, exo-2,3-epoxynorbornane, bis (3,4-epoxy-6-methylcyclohexylmethyl) adipate, 2- (7-oxabicyclo [4.1.0] hept-3- Yl) -spiro (1,3-dioxane-5,3 ′-[7] oxabicyclo [4.1.0] heptane, 4- (1′-methylepoxyethyl) -1,2-epoxy-2-methyl Examples include cyclohexane and 4-epoxyethyl-1,2-epoxycyclohexane.

  (7) Specific examples of the epoxidized fatty acid monoester include esters of an epoxidized fatty acid having 12 to 20 carbon atoms with an alcohol or phenol having 1 to 8 carbon atoms or an alkylphenol. In particular, butyl, hexyl, benzyl, cyclohexyl, methoxyethyl, octyl, phenyl and butylphenyl esters of epoxy stearate are preferably used.

  (8) Specific examples of epoxidized vegetable oils include epoxy compounds of vegetable oils such as soybean oil, linseed oil, and cottonseed oil.

  When the epoxy compound as the component (G) is blended in the lubricating oil composition for paper machine of the present invention, the blending amount is not particularly limited, but is usually based on the total amount of the lubricating oil composition for paper machine (base oil and It is desirable to add an epoxy compound in such an amount that the content thereof is 0.1 to 5.0% by mass, more preferably 0.2 to 2.0% by mass based on the total amount of all formulation additives. .

(H) component:
Although it is an optional component, the lubricating oil composition for paper machine of the present invention has (HA) component as (HA) phenol-based antioxidant and (H-B) amine-based oxidation from the viewpoint of oxidation stability. An inhibitor, or both, can be included.
As the (HA) phenolic antioxidant, any phenolic compound used as an antioxidant for lubricating oil can be used, and is not particularly limited. For example, the following general formula One or more alkylphenol compounds selected from the compounds represented by (31) or the general formula (32) are preferred.

In the general formula ^{(31), R 59} represents an alkyl group having 1 to 4 carbon ^{atoms, R 60} represents a hydrogen atom or an alkyl group having 1 to 4 carbon ^{atoms, R 61} is a hydrogen atom, 1 to 4 carbon atoms An alkyl group, a group represented by the following general formula (31-i) or a group represented by the following general formula (31-ii).

In the general formula ^{(31-i), R 62} is an alkylene group having 1 to 6 carbon atoms, also ^{R 63} represents an alkyl or alkenyl group having 1 to 24 carbon atoms.

In the general formula ^{(31-ii), R 64} represents an alkylene group having 1 to 6 carbon ^{atoms, R 65} represents an alkyl group having 1 to 4 carbon ^{atoms, R 66} is a hydrogen atom or 1 to 4 carbon atoms An alkyl group is shown.

In the general formula (32), R ⁶⁷ and R ⁷¹ each independently represent an alkyl group having 1 to 4 carbon atoms, and R ⁶⁸ and R ⁷² each independently represent a hydrogen atom or a carbon atom having 1 to 4 carbon atoms. Represents an alkyl group, R ⁶⁹ and R ⁷⁰ each independently represent an alkylene group having 1 to 6 carbon atoms, and X ⁸ represents an alkylene group having 1 to 18 carbon atoms or the following general formula (32-i). The group to be shown is shown.

In the general formula (32-i), R ⁷³ and R ⁷⁴ each independently represent an alkylene group having 1 to 6 carbon atoms.

In the general formula (31), R ⁵⁹ is specifically methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, etc. Although mentioned, a tert- butyl group is preferable from the point which is excellent in oxidation stability. Examples of R ⁶⁰ include a hydrogen atom or an alkyl group having 1 to 4 carbon atoms as described above, and a methyl group or a tert-butyl group is preferable from the viewpoint of excellent oxidation stability.

In the general formula (31), when R ⁶¹ is an alkyl group having 1 to 4 carbon atoms, specifically, as R ⁶¹ , a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, An isobutyl group, a sec-butyl group, a tert-butyl group, and the like can be mentioned. From the viewpoint of excellent oxidation stability, a methyl group or an ethyl group is preferable.

Of the alkylphenol compounds represented by the general formula (31), particularly preferred as a compound when R ⁶¹ is an alkyl group having 1 to 4 carbon atoms is 2,6-di-tert-butyl-p-cresol. 2,6-di-tert-butyl-4-ethylphenol and mixtures thereof.

In the case where R ⁶¹ in the general formula (31) is a group represented by the general formula (31-i), the alkylene group having 1 to 6 carbon atoms represented by R ⁶² in the general formula (31-i) is: It may be linear or branched. Specifically, for example, methylene group, methylmethylene group, ethylene group (dimethylene group), ethylmethylene group, propylene group (methylethylene group), trimethylene group, linear chain Or a branched butylene group, a linear or branched pentylene group, a linear or branched hexylene group, etc. are mentioned.

R ⁶² is an alkylene group having 1 to 2 carbon atoms, specifically, for example, a methylene group, a methylmethylene group, an ethylene group (dimethylene group) in that the compound represented by the general formula (31) can be produced with a small number of reaction steps. Etc. are more preferable.

On the other hand, the alkyl group or alkenyl group having 1 to 24 carbon atoms represented by R ⁶³ in the general formula (31-i) may be linear or branched, and specifically includes, for example, methyl group, ethyl group Propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group Group, icosyl group, henicosyl group, docosyl group, tricosyl group, tetracosyl group and the like (these alkyl groups may be linear or branched); vinyl group, propenyl group, isopropenyl group, butenyl group, Pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dopenyl Decenyl group, tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group, heptadecenyl group, octadecenyl group, octadecadienyl group, nonadecenyl group, icocenyl group, heicosenyl group, dococenyl group, tricocenyl group, tetracocenyl group, etc. The alkenyl group may be linear or branched, and the position of the double bond is arbitrary).

R ⁶³ is an alkyl group having 4 to 18 carbon atoms, specifically, for example, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, because of its excellent solubility in base oils. Alkyl groups such as undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group (these alkyl groups may be linear or branched) and have 6 carbon atoms. A linear or branched alkyl group having ˜12 is more preferable, and a branched alkyl group having 6 to 12 carbon atoms is particularly preferable.

Among the phenol compounds represented by the general formula (31), as a compound when R ⁶¹ is a group represented by the general formula (31-i), R ⁶² in the general formula (31-i) is carbon. More preferably, it is an alkylene group having 1 or 2 and R ⁶³ is a linear or branched alkyl group having 6 to 12 carbon atoms, and R ⁶² in the general formula (31-i) has 1 to 2 carbon atoms. Particularly preferred is an alkylene group having 2 and R ⁶³ is a branched alkyl group having 6 to 12 carbon atoms.

  More specific examples of the more preferable compound include (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate n-hexyl, (3-methyl-5-tert-butyl-4-hydroxyphenyl) isohexyl acetate, N-heptyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, isoheptyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, (3-methyl-5-tert-butyl) -4-hydroxyphenyl) acetic acid n-octyl, (3-methyl-5-tert-butyl-4-hydroxyphenyl) isooctyl acetate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetic acid 2-ethylhexyl , (3-Methyl-5-tert-butyl-4-hydroxyphenyl) acetic acid n-no , Isononyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, n-decyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, (3-methyl-5-tert -Butyl-4-hydroxyphenyl) isodecyl acetate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) n-undecyl acetate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) isoundecyl acetate N-dodecyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, isododecyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) acetate, (3-methyl-5-tert- N-hexyl butyl-4-hydroxyphenyl) propionate, (3-methyl-5-tert-butyl) 4-Hydroxyphenyl) isohexyl propionate, n-heptyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) propion Isoheptyl acid, n-octyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate, isooctyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate, (3-methyl- 5-tert-butyl-4-hydroxyphenyl) propionic acid 2-ethylhexyl, (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionic acid n-nonyl, (3-methyl-5-tert-butyl- 4-hydroxyphenyl) isononyl propionate, (3-methyl N-decyl til-5-tert-butyl-4-hydroxyphenyl) propionate, isodecyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate, (3-methyl-5-tert-butyl- 4-hydroxyphenyl) n-undecyl propionate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) isoundecyl propionate, (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate n -Dodecyl, isododecyl (3-methyl-5-tert-butyl-4-hydroxyphenyl) propionate, (3,5-di-tert-butyl-4-hydroxyphenyl) acetate n-hexyl, (3,5-di-) -Tert-butyl-4-hydroxyphenyl) isohexyl acetate, (3,5- -Tert-butyl-4-hydroxyphenyl) acetic acid n-heptyl, (3,5-di-tert-butyl-4-hydroxyphenyl) isoheptyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) N-octyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) isooctyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) acetic acid 2-ethylhexyl, (3,5- N-nonyl di-tert-butyl-4-hydroxyphenyl) acetate, isononyl (3,5-di-tert-butyl-4-hydroxyphenyl) acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) ) N-decyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) isodecyl acetate, (3,5-di-) tert-butyl-4-hydroxyphenyl) acetic acid n-undecyl, (3,5-di-tert-butyl-4-hydroxyphenyl) isoundecyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) acetic acid n-dodecyl, (3,5-di-tert-butyl-4-hydroxyphenyl) isododecyl acetate, (3,5-di-tert-butyl-4-hydroxyphenyl) propionate n-hexyl, (3,5- Di-tert-butyl-4-hydroxyphenyl) isohexyl propionate, n-heptyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, (3,5-di-tert-butyl-4- Hydroxyphenyl) isoheptyl propionate, (3,5-di-tert-butyl-4-hydroxypheny N) -octyl propionate, (3,5-di-tert-butyl-4-hydroxyphenyl) isooctyl propionate, 2-ethylhexyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, N-nonyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, isononyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, (3,5-di-tert -Butyl-4-hydroxyphenyl) n-decyl propionate, (3,5-di-tert-butyl-4-hydroxyphenyl) isodecyl propionate, (3,5-di-tert-butyl-4-hydroxyphenyl) N-undecyl propionate, (3,5-di-tert-butyl-4-hydroxyphenyl) propiate Isoundecylate, n-dodecyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, isododecyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, and mixtures thereof Etc.

In the case where R ⁶¹ in the general formula (31) is a group represented by the general formula (31-ii), R ⁶⁴ in the general formula (31-ii) represents an alkylene group having 1 to 6 carbon atoms. . The alkylene group may be linear or branched, and specific examples include various alkylene groups exemplified above for R ⁶³ . R ⁶⁴ is an alkylene group having 1 to 3 carbon atoms, specifically, for example, a methylene group, a methylmethylene group, ethylene, because the compound of the general formula (31) can be produced by a reaction process with few compounds and its raw materials are easily available. A group (dimethylene group), ethylmethylene group, propylene group (methylethylene group), trimethylene group and the like are more preferable. Specific examples of R ⁶⁵ in the general formula (31-ii) include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. Although a butyl group etc. are mentioned, A tert-butyl group is preferable from the point which is excellent in oxidation stability. Examples of R ⁶⁶ include a hydrogen atom or an alkyl group having 1 to 4 carbon atoms as described above, and a methyl group or a tert-butyl group is preferable from the viewpoint of excellent oxidation stability.

Of the alkylphenol compounds represented by the general formula (31), preferred examples of the compound in the case where R ⁶¹ is a group represented by the general formula (31-ii) are bis (3, 5-di-tert-butyl-4-hydroxyphenyl) methane, 1,1-bis (3,5-di-tert-butyl-4-hydroxyphenyl) ethane, 1,2-bis (3,5-di-) tert-butyl-4-hydroxyphenyl) ethane, 1,1-bis (3,5-di-tert-butyl-4-hydroxyphenyl) propane, 1,2-bis (3,5-di-tert-butyl- 4-hydroxyphenyl) propane, 1,3-bis (3,5-di-tert-butyl-4-hydroxyphenyl) propane, 2,2-bis (3,5-di-tert-butyl-4-hydroxy) Ciphenyl) propane, and mixtures thereof.

On the other hand, in the general formula (32), R ⁶⁷ and R ⁷¹ are each independently an alkyl group having 1 to 4 carbon atoms, specifically, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, n-Butyl group, isobutyl group, sec-butyl group, tert-butyl group and the like are shown, and from the viewpoint of excellent oxidation stability, both are preferably tert-butyl groups. R ⁶⁸ and R ⁷² are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms as described above. From the viewpoint of excellent oxidation stability, each of R ⁶⁸ and R ⁷² is independently a methyl group or tert. -It is preferably a butyl group.

In the general formula (32), the alkylene group having 1 to 6 carbon atoms, which represents R ⁶⁹ and R ⁷⁰ , may be linear or branched. ^The various alkylene groups mentioned above about ⁶² are mentioned. R ⁶⁹ and R ⁷⁰ are each independently an alkylene group having 1 to 2 carbon atoms, in that the compound represented by the general formula (32) can be produced in a reaction process with few compounds and the raw materials are easy to obtain. Specifically, for example, a methylene group, a methylmethylene group, an ethylene group (dimethylene group) and the like are more preferable.

In the general formula (32), the alkylene group having 1 to 18 carbon atoms shows the X ^8, and specific examples include a methylene group, methyl methylene group, ethylene group (dimethylene group), ethyl methylene group, propylene group (Methylethylene group), trimethylene group, butylene group, pentylene group, hexylene group, heptylene group, octylene group, nonylene group, decylene group, undecylene group, dodecylene group, tridecylene group, tetradecylene group, pentadecylene group, hexadecylene group, heptadecylene group , Octadecylene groups and the like (these alkylene groups may be linear or branched). From the viewpoint of easy availability of raw materials, an alkylene group having 1 to 6 carbon atoms, specifically, for example, a methylene group , Methylmethylene group, ethylene group (dimethylene group), ethylmethylene group, pro Pyrene group (methylethylene group), trimethylene group, butylene group, pentylene group, hexylene group and the like (these alkylene groups may be linear or branched) are more preferable, ethylene group (dimethylene group), trimethylene group, A linear alkylene group having 2 to 6 carbon atoms such as a linear butylene group (tetramethylene group, linear pentylene group (pentamethylene group), linear hexylene group (hexamethylene group), etc. is particularly preferred. Of the alkylphenol compounds represented, a compound represented by the following formula (33) is particularly preferable as a compound when X ⁸ is an alkylene group having 1 to 18 carbon atoms.

In addition, when X ⁸ in the general formula (32) is a group represented by the general formula (32-i), the number of carbon atoms represented by R ⁷³ and R ⁷⁴ in the general formula (32-i) is 1 to The alkylene group 6 may be linear or branched, and specific examples include various alkylene groups as described above for R ⁶² individually. R ⁷³ and R ⁷⁴ are each individually an alkylene group having 1 to 3 carbon atoms, specifically, for example, a methylene group, More preferred are methylene group, ethylene group (dimethylene group), ethylmethylene group, propylene group (methylethylene group), trimethylene group and the like. Of the alkylphenols represented by the general formula (32), those particularly preferred as the compound when X ⁸ is a group represented by the general formula (32-i) are compounds represented by the following formula (34) It is.

  As a matter of course, the (HA) component of the optional component of the present invention is one compound selected from alkylphenol compounds represented by the general formula (31) and the general formula (32). May be used alone, or a mixture of two or more compounds selected from the above in an arbitrary mixing ratio may be used.

  The upper limit of the (HA) component in the lubricating oil composition for a paper machine of the present invention is 3% by mass, preferably 2% by mass, more preferably 1% by mass based on the total amount of the composition. Even if the content exceeds 3% by mass, oxidation stability sufficient to meet the content and further improvement of the sludge formation inhibiting effect are not observed, and solubility in the base oil decreases, which is not preferable.

  On the other hand, the lower limit of the content of the component (H) is 0.01% by mass, preferably 0.1% by mass, and more preferably 0.2% by mass based on the total amount of the composition. When the content of the (HA) component is less than 0.01% by mass, the effect of addition is not observed, and the oxidation stability and sludge generation suppressing effect of the lubricating oil composition for paper machine may be deteriorated. This is not preferable.

  As the (H-B) amine-based antioxidant in the (H) component that can be added as an optional component, any amine-based compound used as an antioxidant for lubricating oils can be used, and is particularly limited. However, it is selected from, for example, (Np-alkyl) phenyl-α-naphthylamine represented by the following general formula (35) or p, p′-dialkyldiphenylamine represented by the general formula (36) One type or two or more types of aromatic amines are preferable.

In the above general formula (35), R ⁷⁵ represents a hydrogen atom or an alkyl group having 1 to 16 carbon atoms.

In the general formula (36), R ⁷⁶ and R ⁷⁷ each independently represent an alkyl group having 1 to 16 carbon atoms.

In the general formula (35) representing (Np-alkyl) phenyl-α-naphthylamine, R ⁷⁵ represents a hydrogen atom or a linear or branched alkyl group having 1 to 16 carbon atoms. The proportion of the functional group occupying in the molecule in the case where the number of carbon atoms of R ⁷⁵ exceeds 16 decreases, there is a possibility that the antioxidant capability is weakened. The alkyl group of R ^75, specifically, for example, a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, A tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group and the like (these alkyl groups may be linear or branched).

Among the compounds represented by the general formula (35), when R ⁷⁵ is an alkyl group, a branched alkyl group having 8 to 16 carbon atoms is preferable because of its excellent solubility of the oxidation product itself in the base oil. Further, a branched alkyl group having 8 to 16 carbon atoms derived from an oligomer of an olefin having 3 or 4 carbon atoms is more preferable. Specific examples of the olefin having 3 or 4 carbon atoms include propylene, 1-butene, 2-butene, and isobutylene. From the viewpoint of excellent solubility of the oxidation product itself in the base oil, Propylene or isobutylene is preferred.

When (Np-alkyl) phenyl-α-naphthylamine represented by the above general formula (35) is used as the amine-based antioxidant (HB) component, R ⁷⁵ is a hydrogen molecule or a dimer of isobutylene. Branched octyl group derived from propylene, branched nonyl group derived from propylene trimer, branched dodecyl group derived from isobutylene trimer, branched dodecyl group derived from propylene tetramer Or a branched pentadecyl group derived from a pentamer of propylene is particularly preferred, a branched octyl group derived from a hydrogen molecule or a dimer of isobutylene, a branched dodecyl group or propylene derived from a trimer of isobutylene The branched dodecyl group derived from the tetramer of is particularly preferred.

When Np-alkylphenyl-α-naphthylamine in which R ⁷⁵ is an alkyl group is used as the aromatic amine represented by the general formula (35), this Np-alkylphenyl-α-naphthylamine is commercially available. A thing may be used. In addition, phenyl-α-naphthylamine and a halogenated alkyl compound having 1 to 16 carbon atoms, an olefin having 2 to 16 carbon atoms, or an olefin oligomer having 2 to 16 carbon atoms and phenyl-α-naphthylamine using a Friedel-Crafts catalyst. It can be easily synthesized by reacting. Specific examples of Friedel-Crafts catalysts in this case include metal halides such as aluminum chloride, zinc chloride, and iron chloride; sulfuric acid, phosphoric acid, phosphorus pentoxide, boron fluoride, acidic clay, activated clay, etc. Or an acidic catalyst.

On the other hand, in the general formula (36) representing p, p′-dialkyldiphenylamine, R ⁷⁶ and R ⁷⁷ each independently represents an alkyl group having 1 to 16 carbon atoms. When one or both of R ⁷⁶ and R ⁷⁷ are hydrogen atoms, they themselves may precipitate as sludge due to oxidation. On the other hand, when the number of carbon atoms exceeds 16, the proportion of functional groups in the molecule is small. Therefore, the antioxidant ability may be weakened.

Specific examples of R ⁷⁶ and R ⁷⁷ include, for example, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, A tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group and the like (these alkyl groups may be linear or branched). Among these, as R ⁷⁶ and R ⁷⁷ , a branched alkyl group having 3 to 16 carbon atoms is preferable from the viewpoint of excellent solubility of the oxidation product itself in the base oil, and further an olefin having 3 or 4 carbon atoms, Alternatively, a branched alkyl group having 3 to 16 carbon atoms derived from the oligomer is more preferable. Specific examples of the olefin having 3 or 4 carbon atoms include propylene, 1-butene, 2-butene, and isobutylene, but the solubility of its own oxidation product in a lubricating base oil is excellent. From the viewpoint, propylene or isobutylene is preferable.

When p, p′-dialkyldiphenylamine represented by the above general formula (36) is used as the amine-based antioxidant (H-B) component, R ⁷⁶ and R ⁷⁷ are isopropyl groups derived from propylene and isobutylene. A tert-butyl group derived, a branched hexyl group derived from a dimer of propylene, a branched octyl group derived from a dimer of isobutylene, a branched nonyl group derived from a trimer of propylene, A branched dodecyl group derived from a trimer of isobutylene, a branched dodecyl group derived from a tetramer of propylene or a branched pentadecyl group derived from a pentamer of propylene is particularly preferred, and is derived from isobutylene. tert-Butyl group, branched hexyl group derived from propylene dimer, derived from dimer of isobutylene Branched octyl, branched nonyl group derived from propylene trimer, is a branched dodecyl group derived from a tetramer of a branched dodecyl or propylene derived from a trimer of isobutylene particularly preferred.

  A commercially available product may be used as the p, p'-dialkyldiphenylamine represented by the general formula (36). Further, similarly to the Np-alkylphenyl-α-naphthylamine represented by the general formula (35), diphenylamine and a halogenated alkyl compound having 1 to 16 carbon atoms, an olefin having 2 to 16 carbon atoms, or 2 to 2 carbon atoms. It can be easily synthesized by reacting 16 olefins or their oligomers with diphenylamine using a Friedel-Crafts catalyst. As the Friedel-Crafts catalyst in this case, specifically, for example, metal halides and acidic catalysts listed in the synthesis of Np-alkylphenyl-α-naphthylamine are used. As a matter of course, the component (H) as an optional component of the present invention includes one compound selected from the aromatic amines represented by the general formula (35) and the general formula (36). You may use independently, Furthermore, you may use the mixture etc. in the arbitrary mixing ratios of 2 or more types of compounds chosen from the above.

  The upper limit of the content of the (HB) amine antioxidant in the lubricating oil composition for paper machine of the present invention is 3% by mass, preferably 2% by mass, more preferably 1% by mass based on the total amount of the composition. %. Even if the content exceeds 3% by mass, further improvement in oxidation stability and sludge formation inhibiting effect commensurate with the content is not seen, and solubility in the base oil decreases, which is not preferable. On the other hand, the lower limit of the content of (H-B) amine-based antioxidant is 0.01% by mass, preferably 0.1% by mass, more preferably 0.2% by mass, based on the total amount of the composition. . When the content of the (H-B) amine antioxidant is less than 0.01% by mass, the effect of addition is not seen, and the oxidation stability and sludge generation inhibitory effect of the lubricating oil composition for paper machine This is not preferable because it may deteriorate.

(I) Component:
Although it is an optional component, it may contain (I) a phosphorus compound as component (I) in order to improve extreme pressure of the lubricating oil composition for paper machine of the present invention.
Specific examples of the phosphorus compound that can be contained herein include phosphoric acid esters such as phosphoric acid monoesters, phosphoric acid diesters, and phosphoric acid triesters; phosphorous acid monoesters, phosphorous acid diesters, Examples thereof include phosphites such as phosphite triesters; salts of these phosphate esters and phosphites; and mixtures thereof. The above-mentioned phosphate esters and phosphites are compounds containing a hydrocarbon group usually having 2 to 30 carbon atoms, preferably 3 to 20 carbon atoms.

  Specific examples of the hydrocarbon group having 2 to 30 carbon atoms include ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, and dodecyl. Group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, etc. (these alkyl groups may be linear or branched); butenyl group, pentenyl group, hexenyl group, heptenyl group Alkenyl groups such as octenyl group, nonenyl group, decenyl group, undecenyl group, dodecenyl group, tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group, heptadecenyl group and octadecenyl group (these alkenyl groups may be linear or branched) Good, and the position of the double bond is arbitrary); C5-C7 cycloalkyl group such as pentyl group, cyclohexyl group, cycloheptyl group; methylcyclopentyl group, dimethylcyclopentyl group, methylethylcyclopentyl group, diethylcyclopentyl group, methylcyclohexyl group, dimethylcyclohexyl group, methylethylcyclohexyl group Alkylcycloalkyl groups having 6 to 11 carbon atoms such as diethylcyclohexyl group, methylcycloheptyl group, dimethylcycloheptyl group, methylethylcycloheptyl group, and diethylcycloheptyl group (the substitution position of the alkyl group to the cycloalkyl group is also arbitrary) Aryl groups such as phenyl group and naphthyl group: tolyl group, xylyl group, ethylphenyl group, propylphenyl group, butylphenyl group, pentylphenyl group, hexylphenyl group, heptyl Each alkylaryl group having 7 to 18 carbon atoms such as an phenyl group, an octylphenyl group, a nonylphenyl group, a decylphenyl group, an undecylphenyl group, a dodecylphenyl group (the alkyl group may be linear or branched, The substitution position on the aryl group is also arbitrary); each arylalkyl group having 7 to 12 carbon atoms such as benzyl group, phenylethyl group, phenylpropyl group, phenylbutyl group, phenylpentyl group, phenylhexyl group (these alkyl groups) May be linear or branched).

  As the phosphorus compound (I) component as an optional component that may be contained, preferred compounds include, for example, monopropyl phosphate, monobutyl phosphate, monopentyl phosphate, monohexyl phosphate, monopeptyl phosphate, mono Phosphoric acid monoalkyl esters such as octyl phosphate (the alkyl group may be linear or branched); Phosphoric acid mono (alkyl) aryl esters such as monophenyl phosphate and monocresyl phosphate; dipropyl phosphate, dibutyl phosphate, Dialkyl phosphates such as dipentyl phosphate, dihexyl phosphate, dipeptyl phosphate and dioctyl phosphate (the alkyl group may be linear or branched); diphenyl phosphate, dicresyl phosphate Phosphoric acid di (alkyl) aryl esters such as tripropyl phosphate, tributyl phosphate, tripentyl phosphate, trihexyl phosphate, tripeptyl phosphate, trioctyl phosphate, etc. May be branched); tri (alkyl) aryl phosphates such as triphenyl phosphate and tricresyl phosphate; monopropyl phosphite, monobutyl phosphite, monopentyl phosphite, monohexyl phosphite, monopeptyl phosphine Phosphite monoalkyl esters such as phyte and monooctyl phosphite (the alkyl group may be linear or branched); Monophenyl phosphite and monocresyl phosphite ) Aryl esters; dialkyl phosphites such as dipropyl phosphite, dibutyl phosphite, dipentyl phosphite, dihexyl phosphite, dipeptyl phosphite, dioctyl phosphite (the alkyl group may be linear or branched) Good); di (alkyl) aryl phosphites such as diphenyl phosphite and dicresyl phosphite; tripropyl phosphite, tributyl phosphite, tripentyl phosphite, trihexyl phosphite, tripeptyl phosphite, trioctyl Trialkyl phosphites such as phosphites (the alkyl group may be linear or branched); tri (alkyl) aryl phosphites such as triphenyl phosphites and tricresyl phosphites; and these Mixture etc. Is mentioned.

  Specific examples of the salts of the phosphoric acid esters and phosphite esters described above include phosphoric acid monoesters, phosphoric acid diesters, phosphorous acid monoesters, phosphorous acid diester esters, ammonia, carbon Examples include salts obtained by allowing a nitrogen-containing compound such as an amine compound containing only a hydrocarbon group of 1 to 8 or a hydroxyl group-containing hydrocarbon group in the molecule to act to neutralize part or all of the remaining acidic hydrogen. It is done.

  Specific examples of the nitrogen-containing compound include ammonia; monomethylamine, monoethylamine, monopropylamine, monobutylamine, monopentylamine, monohexylamine, monoheptylamine, monooctylamine, dimethylamine, methylethylamine, Alkylamines such as diethylamine, methylpropylamine, ethylpropylamine, dipropylamine, methylbutylamine, ethylbutylamine, propylbutylamine, dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, etc. May be branched); monomethanolamine, monoethanolamine, monopropanolamine, monobutanolamine, monopentanolamine, monohexanolamine , Monoheptanolamine, monooctanolamine, monononanolamine, dimethanolamine, methanolethanolamine, diethanolamine, methanolpropanolamine, ethanolpropanolamine, dipropanolamine, methanolbutanolamine, ethanolbutanolamine, propanolbutanolamine, dibutanol And alkanolamines such as amines, dipentanolamines, dihexanolamines, diheptanolamines, dioctanolamines (the alkanol groups may be linear or branched); and mixtures thereof.

  As a matter of course, the phosphorus compound which may be contained as the component (I) is one compound selected from the above-mentioned phosphate esters, phosphites, salts thereof and the like. May be used alone, or a mixture of two or more compounds selected from the above in an arbitrary mixing ratio may be used.

  The upper limit of the content of the phosphorus compound in the paper machine lubricating oil composition of the present invention is 10% by mass, preferably 5% by mass, more preferably 3% by mass, based on the total amount of the composition. Even if the content exceeds 5% by mass, no further improvement in lubricity corresponding to the content is observed and oxidation stability is lowered, which is not preferable. On the other hand, the lower limit of the phosphorus compound content is 0.01% by mass, preferably 0.05% by mass, and more preferably 0.1% by mass, based on the total amount of the composition. When the content of the phosphorus compound is less than 0.01% by mass, the effect of addition is hardly exhibited.

(J) Component:
Although it is an optional component, an oily agent can be added as the component (J) to the lubricating oil composition for a paper machine of the present invention from the viewpoint of improving friction characteristics.
Examples of oil agents include ester oil agents, alcohol oil agents, carboxylic acid oil agents, ether oil agents, amine oil agents, amide oil agents, and the like.

  The ester oily agent is obtained by reacting an alcohol and a carboxylic acid. The alcohol may be a monohydric alcohol or a polyhydric alcohol. The carboxylic acid may be a monobasic acid or a polybasic acid.

  As the monohydric alcohol constituting the ester oil-based agent, those having 1 to 24 carbon atoms, preferably 1 to 12 carbon atoms, more preferably 1 to 8 carbon atoms are usually used. May be saturated, saturated or unsaturated. Specific examples of the alcohol having 1 to 24 carbon atoms include methanol, ethanol, linear or branched propanol, linear or branched butanol, linear or branched pentanol, and linear Linear or branched hexanol, linear or branched heptanol, linear or branched octanol, linear or branched nonanol, linear or branched decanol, linear or branched Undecanol, linear or branched dodecanol, linear or branched tridecanol, linear or branched tetradecanol, linear or branched pentadecanol, linear or branched hexadecane Decanol, linear or branched heptadecanol, linear or branched octadecanol, linear or branched nonadecanol, linear or branched icosa Lumpur, linear or branched Hen'ikosanoru, linear or branched Torikosanoru, such as linear or branched tetracosanol, and mixtures thereof.

  Moreover, as a polyhydric alcohol which comprises ester oiliness agent, a 2-10 valence is used normally, Preferably a 2-6 valence is used. Specific examples of the 2 to 10 polyhydric alcohol include, for example, ethylene glycol, diethylene glycol, polyethylene glycol (3 to 15 mer of ethylene glycol), propylene glycol, dipropylene glycol, and polypropylene glycol (3 to 15 of propylene glycol). Monomer), 1,3-propanediol, 1,2-propanediol, 1,3-butanediol, 1,4-butanediol, 2-methyl-1,2-propanediol, 2-methyl-1,3 -Dihydric alcohols such as propanediol, 1,2-pentanediol, 1,3-pentanediol, 1,4-pentanediol, 1,5-pentanediol, neopentylglycol; glycerin, polyglycerin (glycerin 2- Octamers such as diglycerin, triglyceride Phosphorus, tetraglycerin, etc.), trimethylol alkanes (trimethylol ethane, trimethylol propane, trimethylol butane, etc.) and their 2- to 8-mer, pentaerythritol and their 2- to 4-mer, 1,2,4- Butanetriol, 1,3,5-pentanetriol, 1,2,6-hexanetriol, 1,2,3,4-butanetetrol, sorbitol, sorbitan, sorbitol glycerin condensate, adonitol, arabitol, xylitol, mannitol, etc. Polyhydric alcohols; sugars such as xylose, arabinose, ribose, rhamnose, glucose, fructose, galactose, mannose, sorbose, cellobiose, maltose, isomaltose, trehalose, sucrose, and mixtures thereof That.

  Among these polyhydric alcohols, ethylene glycol, diethylene glycol, polyethylene glycol (ethylene glycol 3-10 mer), propylene glycol, dipropylene glycol, polypropylene glycol (propylene glycol 3-10 mer), 1,3- Propanediol, 2-methyl-1,2-propanediol, 2-methyl-1,3-propanediol, neopentyl glycol, glycerin, diglycerin, triglycerin, trimethylolalkane (trimethylolethane, trimethylolpropane, trimethylol Methylol butane and the like, and dimers and tetramers thereof, pentaerythritol, dipentaerythritol, 1,2,4-butanetriol, 1,3,5-pentanetriol, 1,2,6-hexanetriol , 1,2,3,4 butane tetrol, sorbitol, sorbitan, sorbitol glycerin condensate, adonitol, arabitol, xylitol, divalent to hexavalent polyhydric alcohols and mixtures thereof, such as mannitol and the like are preferable. Even more preferred are ethylene glycol, propylene glycol, neopentyl glycol, glycerin, trimethylol ethane, trimethylol propane, pentaerythritol, sorbitan, and mixtures thereof.

  The alcohol constituting the ester oil agent according to the component (J) of the present invention may be a monohydric alcohol or a polyhydric alcohol as described above. It is preferable that

  Of the acids constituting the ester oily agent according to the component (J) of the present invention, as the monobasic acid, a fatty acid having 2 to 24 carbon atoms is usually used, and the fatty acid is linear or branched. It may be saturated or unsaturated. Specifically, for example, acetic acid, propionic acid, linear or branched butanoic acid, linear or branched pentanoic acid, linear or branched hexanoic acid, linear or branched heptane Acid, linear or branched octanoic acid, linear or branched nonanoic acid, linear or branched decanoic acid, linear or branched undecanoic acid, linear or branched dodecane Acid, linear or branched tridecanoic acid, linear or branched tetradecanoic acid, linear or branched pentadecanoic acid, linear or branched hexadecanoic acid, linear or branched heptadecane Acid, linear or branched octadecanoic acid, linear or branched hydroxyoctadecanoic acid, linear or branched nonadecanoic acid, linear or branched icosanoic acid, linear or branched Henicosanoic acid, linear or branched Saturated fatty acids such as cosanoic acid, linear or branched tricosanoic acid, linear or branched tetracosanoic acid, acrylic acid, linear or branched butenoic acid, linear or branched pentenoic acid, Linear or branched hexenoic acid, linear or branched heptenoic acid, linear or branched octenoic acid, linear or branched nonenoic acid, linear or branched decenoic acid, Linear or branched undecenoic acid, linear or branched dodecenoic acid, linear or branched tridecenoic acid, linear or branched tetradecenoic acid, linear or branched pentadecenoic acid, Linear or branched hexadecenoic acid, linear or branched heptadecenoic acid, linear or branched octadecenoic acid, linear or branched hydroxyoctadecenoic acid, linear or branched nonadecene Acid, linear or branched Unsaturated fatty acids such as cocenoic acid, linear or branched heicosenoic acid, linear or branched docosenoic acid, linear or branched tricosenoic acid, linear or branched tetracosenoic acid, and the like And the like.

  Examples of the polybasic acid include dibasic acid and trimellitic acid, and dibasic acid is preferable. The dibasic acid may be a chain dibasic acid or a cyclic dibasic acid. Further, in the case of a chain dibasic acid, it may be either linear or branched, and may be either saturated or unsaturated. The chain dibasic acid is preferably a chain dibasic acid having 2 to 16 carbon atoms. Specifically, for example, ethanedioic acid, propanedioic acid, linear or branched butanedioic acid, linear Or branched pentanedioic acid, linear or branched hexanedioic acid, linear or branched heptanedioic acid, linear or branched octanedioic acid, linear or branched nonane diacid Acid, linear or branched decanedioic acid, linear or branched undecanedioic acid, linear or branched dodecanedioic acid, linear or branched tridecanedioic acid, linear or Branched tetradecanedioic acid, linear or branched heptadecanedioic acid, linear or branched hexadecanedioic acid, linear or branched hexenedioic acid, linear or branched heptenedioic acid Linear or branched octene diacid, linear or branched nonene diacid, linear or branched Branched decenedioic acid, linear or branched undecenedioic acid, linear or branched dodecenedioic acid, linear or branched tridecenedioic acid, linear or branched tetradecenedioic acid And linear or branched heptacene diacid, linear or branched hexadecene diacid, and mixtures thereof. Examples of the cyclic dibasic acid include 1,2-cyclohexanedicarboxylic acid, 4-cyclohexene-1,2-dicarboxylic acid, and aromatic dicarboxylic acid. Among these, a chain dibasic acid is preferable from the viewpoint of stability.

  The acid constituting the ester oily agent may be a monobasic acid or a polybasic acid as described above, but a monobasic acid is preferred from the viewpoint that the effect of improving friction characteristics is more excellent.

  The combination of the alcohol and the acid in the ester-based oily agent is arbitrary and is not particularly limited, and examples thereof include esters by the following combinations (i) to (vii).

(I) ester of monohydric alcohol and monobasic acid (ii) ester of polyhydric alcohol and monobasic acid (iii) ester of monohydric alcohol and polybasic acid (iv) polyhydric alcohol and polybasic acid (V) Monohydric alcohol, mixed ester of polyhydric alcohol and polybasic acid (vi) Mixed ester of polyhydric alcohol and monobasic acid, polybasic acid (vii) Monohydric alcohol A mixed ester of a mixture of a polyhydric alcohol and a monobasic acid or polybasic acid.

  Each of the esters (ii) to (vii) may be a complete ester in which all of the hydroxyl groups of the polyhydric alcohol or the carboxyl groups of the polybasic acid are esterified, and some of them are hydroxyl groups or carboxyl groups. The remaining partial ester may be used, but the partial ester is preferable from the viewpoint of the effect of improving the friction characteristics.

  Among the esters (i) to (vii) above, (ii) an ester of a polyhydric alcohol and a monobasic acid is preferable. This ester has a very high effect of improving friction characteristics.

In the ester (ii), the number of carbon atoms of the monobasic acid is preferably 10 or more, more preferably 12 or more, and still more preferably 14 or more, from the viewpoint that the frictional characteristics are further improved.
In addition, the number of carbon atoms of the monobasic acid is preferably 28 or less, more preferably 26 or less, and still more preferably 24 or less, from the viewpoint of preventing precipitation. Examples of such esters include glycerin monooleate and sorbitan monooleate.

  Examples of the alcohol oil-based agent include alcohols exemplified in the description of the ester oil-based agent. The number of carbon atoms in the alcohol oil-based agent is preferably 6 or more, more preferably 8 or more, and most preferably 10 or more, from the viewpoint of improving frictional characteristics. Moreover, since there exists a possibility that it may precipitate easily when carbon number is too large, 24 or less are preferable, 20 or less are more preferable, and 18 or less are the most preferable.

  The carboxylic acid oily agent may be a monobasic acid or a polybasic acid. Examples of such carboxylic acids include monobasic acids and polybasic acids exemplified in the description of the ester oily agent. Among these, a monobasic acid is preferable from the viewpoint of improving the friction characteristics. In addition, the number of carbon atoms of the carboxylic acid oil-based agent is preferably 6 or more, more preferably 8 or more, and most preferably 10 or more from the viewpoint of improving the friction characteristics. Moreover, since there exists a possibility that it may precipitate easily when carbon number of a carboxylic acid oiliness agent is too large, 24 or less are preferable, 20 or less are more preferable, and 18 or less are the most preferable.

  Examples of ether oily agents include etherified products of 3 to 6 aliphatic polyhydric alcohols, bimolecular condensates or trimolecular condensates of 3 to 6 aliphatic polyhydric alcohols, and the like.

［式中、Ｒ^７８〜Ｒ^１０２は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜１８の直鎖状もしくは分岐鎖状のアルキル基、アリル基、アラルキル基、−（Ｒ^aＯ）_n−Ｒ^b（Ｒ^aは炭素数２〜６のアルキレン基、Ｒ^bは炭素数１〜２０のアルキル基、アリル基、アラルキル基、ｎは１〜１０の整数を示す）で示されるグリコールエーテル残基を示す。］ Etherified products of 3 to 6-valent aliphatic polyhydric alcohols are represented, for example, by the following general formulas (37) to (42).

[Wherein, R ^{78 to} R ¹⁰² may be the same or different and each represents a hydrogen atom or a linear or branched alkyl group having 1 to 18 carbon atoms, an allyl group, an aralkyl group, — (R ^a O ) _N -R ^b (R ^a is an alkylene group having 2 to 6 carbon atoms, R ^b is an alkyl group having 1 to 20 carbon atoms, an allyl group, an aralkyl group, and n is an integer of 1 to 10) Indicates an ether residue. ]

Specific examples of the 3-6 valent aliphatic polyhydric alcohol include glycerin, trimethylolpropane, erythritol, pentaerythritol, arabitol, sorbitol, mannitol and the like. R ^{77 to} R ¹⁰¹ in the general formulas (37) to (42) are methyl group, ethyl group, n-propyl group, isopropyl group, various butyl groups, various pentyl groups, various hexyl groups, various heptyl groups, Various octyl groups, various nonyl groups, various decyl groups, various undecyl groups, various dodecyl groups, various tridecyl groups, various tetradecyl groups, various pentadecyl groups, various hexadecyl groups, various heptadecyl groups, various octadecyl groups, phenyl groups, benzyl groups, etc. Is mentioned. The etherified product also includes a partially etherified product in which a part of R ^{77 to} R ¹⁰¹ is a hydrogen atom.

［式中、Ｒ^７８〜Ｒ^８０及びＲ^８８〜Ｒ^９１はそれぞれ式（３７）中のＲ^７７〜Ｒ^７９及び式（４０）中のＲ^８８〜Ｒ^９１と同一の定義内容を示す。］
３〜６価の脂肪族多価アルコールの二分子縮合物，三分子縮合物の具体例としては、ジグリセリン、ジトリメチロールプロパン、ジペンタエリスリトール、ジソルビトール、トリグリセリン、トリトリメチロールプロパン、トリペンタエリスリトール、トリソルビトールなどが挙げられる。 As the etherified product of a bimolecular condensate or a trimolecular condensate of a 3-6 valent aliphatic polyhydric alcohol, the same or different condensates of the compounds represented by the general formulas (37) to (42) are used. Is mentioned. For example, the bimolecular condensate of alcohol and the etherified product of the trimolecular condensate represented by general formula (37) are represented by general formulas (43) and (44), respectively. Moreover, the etherified product of the alcohol bimolecular condensate and trimolecular condensate represented by the general formula (39) is represented by the general formulas (45) and (46), respectively.

Wherein ^indicates the same definition as ^R 88 ^{to R 91} of ^R 77 ^{to R 79} and the formula (40) in R 78 ^{to R 80} and ^R 88 ^{to R 91} each formula (37) in. ]
Specific examples of bimolecular and trimolecular condensates of 3-6 valent aliphatic polyhydric alcohols include diglycerin, ditrimethylolpropane, dipentaerythritol, disorbitol, triglycerin, tritrimethylolpropane, and tripentaerythritol. And trisorbitol.

Specific examples of the ether oil agents represented by the general formulas (37) to (46) include glycerin trihexyl ether, glycerin dimethyl octyl triether, glycerin di (methyloxyisopropylene) dodecyl triether, and glycerin. Diphenyl octyl triether, di (phenyloxyisopropylene) dodecyl triether of glycerin, trihexyl ether of trimethylol propane, dimethyl octyl triether of trimethylol propane, di (methyloxy isopropylene) dodecyl triether of trimethylol propane, Tetrahexyl ether of pentaerythritol, trimethyloctyl tetraether of pentaerythritol, tri (methyloxyisopropylene) dodecylte of pentaerythritol Laether, Hexapropyl ether of sorbitol, Tetramethyloctylpentaether of sorbitol, Hexa (methyloxyisopropylene) ether of sorbitol, Tetrabutyl ether of diglycerin, Dimethyldioctyltetraether of diglycerin, Tri (methyloxyisopropylene) ) Dodecyl tetraether, triglycerol pentaethyl ether, triglycerol trimethyldioctylpentaether, triglycerol tetra (methyloxyisopropylene) decylpentaether, ditrimethylolpropane tetrabutylether, ditrimethylolpropane dimethyldioctyltetraether, Tri (methyloxyisopropylene) dodecyltetrae of ditrimethylolpropane Ter, tritrimethylolpropane pentaethyl ether, tritrimethylolpropane trimethyldioctylpentaether, tritrimethylolpropane tetra (methyloxyisopropylene) decylpentaether, dipentaerythritol hexapropylether, dipentaerythritol pentamethyloctylhexa Ether, dipentaerythritol hexa (methyloxyisopropylene) ether, tripentaerythritol octapropyl ether, tripentaerythritol pentamethyloctyl hexaether, tripentaerythritol hexa (methyloxyisopropylene) ether, disorbitol octater Methyl dioctyl deca ether, disorbitol deca (methyloxyisopropylate N) ether.
Among these, diphenyl octyl triether of glycerin, di (methyloxyisopropylene) dodecyl triether of trimethylolpropane, tetrahexyl ether of pentaerythritol, hexapropyl ether of sorbitol, dimethyldioctyl tetraether of diglycerin, triglycerin of triglycerin Tetra (methyloxyisopropylene) decyl pentaether, hexapentyl ether of dipentaerythritol, and pentamethyloctyl hexaether of tripentaerythritol are preferred.

  The oily agent as the component (J) that can be used in the present invention includes (J-1) an amine oily agent and (J-2) an amide oily agent.

  (J-1) Examples of amine oily agents include monoamines, polyamines, and alkanolamines. Among these, monoamines are preferable from the viewpoint of improving frictional properties.

Specific examples of monoamines include monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, monopropylamine (including all isomers), dipropylamine (including all isomers), Propylamine (including all isomers), monobutylamine (including all isomers), dibutylamine (including all isomers), tributylamine (including all isomers), monopentylamine (all including all isomers) Including isomers), dipentylamine (including all isomers), tripentylamine (including all isomers), monohexylamine (including all isomers), dihexylamine (including all isomers) ), Monoheptylamine (including all isomers), diheptylamine (including all isomers) ), Monooctylamine (including all isomers), dioctylamine (including all isomers), monononylamine (including all isomers), monodecylamine (including all isomers), monoundecyl (Including all isomers), monododecylamine (including all isomers), monotridecylamine (including all isomers), monotetradecylamine (including all isomers), monopentadecyl Amine (including all isomers), monohexadecylamine (including all isomers), monoheptadecylamine (including all isomers), monooctadecylamine (including all isomers), mononona Decylamine (including all isomers), monoicosylamine (including all isomers), monohenicosylamine (including all isomers), monodocosyl Min (including all isomers), monotricosylamine (including all isomers), dimethyl (ethyl) amine, dimethyl (propyl) amine (including all isomers), dimethyl (butyl) amine (all Isomers), dimethyl (pentyl) amine (including all isomers), dimethyl (hexyl) amine (including all isomers), dimethyl (heptyl) amine (including all isomers), dimethyl ( Octyl) amine (including all isomers), dimethyl (nonyl) amine (including all isomers), dimethyl (decyl) amine (including all isomers), dimethyl (undecyl) amine (all isomers) ), Dimethyl (dodecyl) amine (including all isomers), dimethyl (tridecyl) amine (including all isomers), dimethyl (tetradecyl) ) Amine (including all isomers), dimethyl (pentadecyl) amine (including all isomers), dimethyl (hexadecyl) amine (including all isomers), dimethyl (heptadecyl) amine (all isomers) ), Dimethyl (octadecyl) amine (including all isomers), dimethyl (nonadecyl) amine (including all isomers), dimethyl (icosyl) amine (including all isomers), dimethyl (henicosyl) Alkylamines such as amines (including all isomers), dimethyl (tricosyl) amine (including all isomers);
Monovinylamine, divinylamine, trivinylamine, monopropenylamine (including all isomers), dipropenylamine (including all isomers), tripropenylamine (including all isomers), monobutenylamine (Including all isomers), dibutenylamine (including all isomers), tributenylamine (including all isomers), monopentenylamine (including all isomers), dipentenylamine (all isomers) ), Tripentenylamine (including all isomers), monohexenylamine (including all isomers), dihexenylamine (including all isomers), monoheptenylamine (all isomers) ), Diheptenylamine (including all isomers), monooctenylamine (including all isomers), dioctenylamine (Including all isomers), monononenylamine (including all isomers), monodecenylamine (including all isomers), monoundecenyl (including all isomers), monododecenylamine (Including all isomers), monotridecenylamine (including all isomers), monotetradecenylamine (including all isomers), monopentadecenylamine (including all isomers), Monohexadecenylamine (including all isomers), monoheptadecenylamine (including all isomers), monooctadecenylamine (including all isomers), monononadecenylamine (all isomers) ), Monoicosenylamine (including all isomers), monohenicocenylamine (including all isomers), monodocosenylamine (including all isomers), Trichoderma cell (including all isomers) cycloalkenyl amines alkenyl amines, such as;
Dimethyl (vinyl) amine, dimethyl (propenyl) amine (including all isomers), dimethyl (butenyl) amine (including all isomers), dimethyl (pentenyl) amine (including all isomers), dimethyl ( Hexenyl) amine (including all isomers), dimethyl (heptenyl) amine (including all isomers), dimethyl (octenyl) amine (including all isomers), dimethyl (nonenyl) amine (all isomers) ), Dimethyl (decenyl) amine (including all isomers), dimethyl (undecenyl) amine (including all isomers), dimethyl (dodecenyl) amine (including all isomers), dimethyl (tridecenyl) Amine (including all isomers), dimethyl (tetradecenyl) amine (including all isomers), dimethyl (pen Decenyl) amine (including all isomers), dimethyl (hexadecenyl) amine (including all isomers), dimethyl (heptadecenyl) amine (including all isomers), dimethyl (octadecenyl) amine (all isomers) ), Dimethyl (nonadecenyl) amine (including all isomers), dimethyl (icosenyl) amine (including all isomers), dimethyl (henicosenyl) amine (including all isomers), dimethyl (tricosenyl) Monoamines having alkyl and alkenyl groups such as amines (including all isomers);
Monobenzylamine, (1-phenyltyl) amine, (2-phenylethyl) amine (also known as monophenethylamine), dibenzylamine, bis (1-phenethyl) amine, bis (2-phenylethylene) amine (also known as diphenethylamine) Aromatic substituted alkylamines such as
C5-C16 cycloalkylamines such as monocyclopentylamine, dicyclopentylamine, tricyclopentylamine, monocyclohexylamine, dicyclohexylamine, monocycloheptylamine, dicycloheptylamine;
Monoamines having an alkyl group and a cycloalkyl group, such as dimethyl (cyclopentyl) amine, dimethyl (cyclohexyl) amine, dimethyl (cycloheptyl) amine;
(Methylcyclopentyl) amine (including all substituted isomers), bis (methylcyclopentyl) amine (including all substituted isomers), (dimethylcyclopentyl) amine (including all substituted isomers), bis (dimethylcyclopentyl) ) Amine (including all substituted isomers), (ethylcyclopentyl) amine (including all substituted isomers), bis (ethylcyclopentyl) amine (including all substituted isomers), (methylethylcyclopentyl) amine ( All substituted isomers included), bis (methylethylcyclopentyl) amine (including all substituted isomers), (diethylcyclopentyl) amine (including all substituted isomers), (methylcyclohexyl) amine (all substituted isomers) Isomers), bis (methylcyclohexyl) amine (all substituted isomers) ), (Dimethylcyclohexyl) amine (including all substituted isomers), bis (dimethylcyclohexyl) amine (including all substituted isomers), (ethylcyclohexyl) amine (including all substituted isomers), bis (Ethylcyclohexyl) amine (including all substituted isomers), (Methylethylcyclohexyl) amine (including all substituted isomers), (Diethylcyclohexyl) amine (including all substituted isomers), (Methylcycloheptyl) ) Amine (including all substituted isomers), bis (methylcycloheptyl) amine (including all substituted isomers), (dimethylcycloheptyl) amine (including all substituted isomers), (ethylcycloheptylamine) (Including all substituted isomers), (methylethylcycloheptyl) amine (all substituted isomers) And alkyl cycloalkylamines such as (diethylcycloheptyl) amine (including all substituted isomers), etc. The monoamine also includes monoamines derived from fats and oils such as beef tallow amine. It is.

  Among the above-mentioned monoamines, alkylamine, monoamine having an alkyl group and an alkenyl group, monoamine having an alkyl group and a cycloalkyl group, cycloalkylamine and alkylcycloalkylamine are particularly preferable from the viewpoint of improving frictional properties, alkylamine, A monoamine having an alkyl group and an alkenyl group is more preferable.

  Although there is no restriction | limiting in particular about carbon number of a monoamine, It is preferable that it is 8 or more from the point of rust prevention property, and it is more preferable that it is 12 or more. Further, from the viewpoint of improving the friction characteristics, it is preferably 24 or less, and more preferably 18 or less.

  Further, the number of hydrocarbon groups bonded to the nitrogen atom in the monoamine is not particularly limited, but is preferably 1 or 2 and more preferably 1 from the viewpoint of improving the frictional characteristics.

  (J-2) As an amide oily agent, an amine compound containing only a fatty acid having 6 to 30 carbon atoms or its acid chloride, ammonia, a hydrocarbon group having 1 to 8 carbon atoms or a hydroxyl group-containing hydrocarbon group in the molecule. An amide obtained by reacting a nitrogen-containing compound such as

  The fatty acid here may be a linear fatty acid or a branched fatty acid, and may be a saturated fatty acid or an unsaturated fatty acid. The carbon number is 6-30, preferably 9-24.

  Specific examples of the fatty acid include heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, Saturated fatty acids such as icosanoic acid, henicosanoic acid, docosanoic acid, tricosanoic acid, tetracosanoic acid, pentacosanoic acid, hexacosanoic acid, heptacosanoic acid, octacosanoic acid, nonacosanoic acid and triacontyl group (these saturated fatty acids may be linear or branched) ); Heptenoic acid, octenoic acid, nonenoic acid, decenoic acid, undecenoic acid, dodecenoic acid, tridecenoic acid, tetradecenoic acid, pentadecenoic acid, hexadecenoic acid, heptadecenoic acid, octadecenoic acid (including oleic acid), nonadecenic acid, icosenic acid Henicosenoic acid Unsaturated fatty acids such as docosenoic acid, tricosenoic acid, tetracosenoic acid, pentacosenoic acid, hexacosenoic acid, heptacosenoic acid, octacosenoic acid, nonacenoic acid, triacontenoic acid (these unsaturated fatty acids may be linear or branched, The position of the heavy bond is also arbitrary); but the linear fatty acids derived from lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, various fats and oils (coconut oil fatty acid etc.) A mixture of linear fatty acid and branched fatty acid synthesized by the oxo method or the like is preferably used.

  Specific examples of the nitrogen-containing compound to be reacted with the fatty acid include ammonia; monomethylamine, monoethylamine, monopropylamine, monobutylamine, monopentylamine, monohexylamine, monoheptylamine, monooctylamine, dimethylamine, Alkylamines such as methylethylamine, diethylamine, methylpropylamine, ethylpropylamine, dipropylamine, methylbutylamine, ethylbutylamine, propylbutylamine, dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, etc. May be chain or branched); monomethanolamine, monoethanolamine, monopropanolamine, monobutanolamine, monopentanolamine, monohexene Noramine, monoheptanolamine, monooctanolamine, monononanolamine, dimethanolamine, methanolethanolamine, diethanolamine, methanolpropanolamine, ethanolpropanolamine, dipropanolamine, methanolbutanolamine, ethanolbutanolamine, propanolbutanolamine, di Examples thereof include alkanolamines such as butanolamine, dipentanolamine, dihexanolamine, diheptanolamine and dioctanolamine (the alkanol group may be linear or branched); and mixtures thereof.

Specific examples of fatty acid amides include lauric acid amide, lauric acid diethanolamide, lauric acid monopropanolamide, myristic acid amide, myristic acid diethanolamide, myristic acid monopropanolamide, palmitic acid amide, palmitic acid diethanolamide, and palmitic acid. Acid monopropanolamide, stearic acid amide, stearic acid diethanolamide, stearic acid monopropanolamide, oleic acid amide, oleic acid diethanolamide, oleic acid monopropanolamide, coconut oil fatty acid amide, coconut oil fatty acid diethanolamide, coconut oil fatty acid mono Propanolamide, Synthetic mixed fatty acid amide having 12 to 13 carbon atoms, Synthetic mixed fatty acid diethanolamide having 12 to 13 carbon atoms, Synthetic mixture having 12 to 13 carbon atoms Fatty acid mono-propanol amides, and mixtures thereof are particularly preferred.
Among the oily agents, preferred are a polyhydric alcohol partial ester and an aliphatic amide from the viewpoint of an effect of improving frictional properties.

  The content of the oily agent as the component (J) is arbitrary, but is preferably 0.01% by mass or more, more preferably 0.05%, based on the total amount of the composition, from the viewpoint of excellent effect of improving the friction characteristics. It is at least mass%, more preferably at least 0.1 mass%. In addition, the content is preferably 10% by mass or less, more preferably 7.5% by mass or less, and further preferably 5% by mass or less, based on the total amount of the composition, from the viewpoint of precipitation prevention.

(K) component:
Although it is an optional component, the lubricating oil composition for paper machine of the present invention contains triazole and / or its derivative represented by the general formula (47) as the component (K) from the viewpoint of improving thermal and oxidation stability. Can be added.

上式中、２つの点線はトリアゾール環に置換する同一または異なる置換基、好ましくは炭化水素基をそれぞれ表し、両者は互いに結合して環状基、たとえば縮合ベンゼン環を構成することができる。
トリアゾールおよび／またはその誘導体として好ましい化合物は、ベンゾトリアゾール及び／又はその誘導体である。

In the above formula, two dotted lines represent the same or different substituents substituted on the triazole ring, preferably a hydrocarbon group, respectively, and both can be bonded to each other to form a cyclic group, for example, a condensed benzene ring.
A preferable compound as triazole and / or a derivative thereof is benzotriazole and / or a derivative thereof.

  As said benzotriazole, the compound represented by following formula (48) is illustrated.

また、ベンゾトリアゾール誘導体としては、例えば、下記一般式（４９）で表されるアルキルベンゾトリアゾールや、一般式（５０）で表される（アルキル）アミノアルキルベンゾトリアゾール等が挙げられる。

Examples of the benzotriazole derivative include alkylbenzotriazole represented by the following general formula (49), (alkyl) aminoalkylbenzotriazole represented by the general formula (50), and the like.

In the above formula (49), R ¹⁰³ represents a linear or branched alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group, and x is 1 to 3, preferably 1 or 2. Indicates the number of Examples of R ¹⁰³ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. As the alkylbenzotriazole represented by the formula (49), a compound in which R ¹⁰³ is a methyl group or an ethyl group and x is 1 or 2 is particularly preferable from the viewpoint of excellent antioxidant properties. Examples thereof include triazole (tolyltriazole), dimethylbenzotriazole, ethylbenzotriazole, ethylmethylbenzotriazole, diethylbenzotriazole, and mixtures thereof.

In the above formula (50), R ¹⁰⁴ represents a linear or branched alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group, R ¹⁰⁵ represents a methylene group or an ethylene group, R ¹⁰⁶ And R ¹⁰⁷ may be the same or different and each represents a hydrogen atom or a linear or branched alkyl group having 1 to 18 carbon atoms, preferably a linear or branched alkyl group having 1 to 12 carbon atoms. Y represents a number of 0 to 3, preferably 0 or 1. Examples of R ¹⁰³ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. R ¹⁰⁶ and R ¹⁰⁷ are, for example, a hydrogen atom, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, straight chain or A branched pentyl group, a linear or branched hexyl group, a linear or branched heptyl group, a linear or branched octyl group, a linear or branched nonyl group, a linear or branched decyl group, Linear or branched undecyl group, linear or branched dodecyl group, linear or branched tridecyl group, linear or branched tetradecyl group, linear or branched pentadecyl group, linear or branched Alkyl groups such as a hexadecyl group, a linear or branched heptadecyl group, and a linear or branched octadecyl group.

As the (alkyl) aminobenzotriazole represented by the above formula (50), R ¹⁰⁴ is a methyl group, y is 0 or 1, and R ¹⁰⁵ is a methylene group or the Dialkylaminoalkylbenzotriazole, dialkylaminoalkyltolyltriazole or a mixture thereof, which is an ethylene group and R ¹⁰⁶ and R ¹⁰⁷ are linear or branched alkyl groups having 1 to 12 carbon atoms, are preferably used. Examples of these dialkylaminoalkylbenzotriazoles include dimethylaminomethylbenzotriazole, diethylaminomethylbenzotriazole, di (linear or branched) propylaminomethylbenzotriazole, and di (linear or branched) butylaminomethylbenzotriazole. , Di (straight or branched) pentylaminomethylbenzotriazole, di (straight or branched) hexylaminomethylbenzotriazole, di (straight or branched) heptylaminomethylbenzotriazole, di (straight or branched) ) Octylaminomethylbenzotriazole, di (straight or branched) nonylaminomethylbenzotriazole, di (straight or branched) decylaminomethylbenzotriazole, di (straight or branched) undecylaminomethylbenzotriazole, (Linear or branched) dodecylaminomethylbenzotriazole; dimethylaminoethylbenzotriazole, diethylaminoethylbenzotriazole, di (linear or branched) propylaminoethylbenzotriazole, di (linear or branched) butylaminoethylbenzo Triazole, di (straight or branched) pentylaminoethylbenzotriazole, di (straight or branched) hexylaminoethylbenzotriazole, di (straight or branched) heptylaminoethylbenzotriazole, di (straight or branched) Branch) Octylaminoethylbenzotriazole, Di (straight or branched) nonylaminoethylbenzotriazole, Di (straight or branched) decylaminoethylbenzotriazole, Di (straight or branched) undecylaminoethylbenzotriazole , Di (linear or straight Branched) dodecylaminoethylbenzotriazole; dimethylaminomethyltolyltriazole, diethylaminomethyltolyltriazole, di (linear or branched) propylaminomethyltolyltriazole, di (straight or branched) butylaminomethyltolyltriazole, di ( Linear or branched) pentylaminomethyltolyltriazole, di (linear or branched) hexylaminomethyltolyltriazole, di (straight or branched) heptylaminomethyltolyltriazole, di (linear or branched) octylamino Methyltolyltriazole, di (linear or branched) nonylaminomethyltolyltriazole, di (straight or branched) decylaminomethyltolyltriazole, di (straight or branched) undecylaminomethyltolyltriazole, di (direct Chain or branch) Silaminomethyltolyltriazole; dimethylaminoethyltolyltriazole, diethylaminoethyltolyltriazole, di (linear or branched) propylaminoethyltolyltriazole, di (linear or branched) butylaminoethyltolyltriazole, di (linear or Branched) pentylaminoethyltolyltriazole, di (straight or branched) hexylaminoethyltolyltriazole, di (straight or branched) heptylaminoethyltolyltriazole, di (straight or branched) octylaminoethyltolyltriazole , Di (linear or branched) nonylaminoethyl tolyl triazole, di (linear or branched) decylaminoethyl tolyl triazole, di (linear or branched) undecylaminoethyl tolyl triazole, di (linear or branched) Branch) Dodecylamino Tilt Lil triazole; or mixtures thereof.

  The content of the triazole and / or derivative thereof as the optional component (K) is arbitrary, but is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, based on the total amount of the composition. is there. When the amount is less than 0.001% by mass, the effect of improving thermal and oxidation stability due to the inclusion of triazole and / or a derivative thereof may be insufficient. Further, the content of triazole and / or a derivative thereof is preferably 1.0% by mass or less, more preferably 0.5% by mass or less, based on the total amount of the composition. When it exceeds 1.0 mass%, there is a possibility that it is economically disadvantageous because the effect of improving the thermal and oxidation stability sufficient for the content cannot be obtained.

Other optional ingredients:
In the present invention, as described above, a lubricating oil composition for a paper machine having excellent extreme pressure can be obtained simply by containing the component (A) and / or the component (B) in the base oil. For the purpose of improving, as necessary, further rust inhibitors, metal deactivators, viscosity index improvers other than (C) dispersion type viscosity index improvers, detergent dispersants, pour point depressants, antifoaming agents Various additives represented by agents and the like may be contained alone or in combination.

  Specific examples of rust inhibitors include metal soaps such as fatty acid metal salts, lanolin fatty acid metal salts, and oxidized wax metal salts; partial alcohol esters such as sorbitan fatty acid esters; esters such as lanolin fatty acid esters; Examples thereof include sulfonates such as calcium sulfonate and barium sulfonate; oxidized wax; amines; phosphoric acid; In the present invention, one or two or more compounds arbitrarily selected from these rust inhibitors can be contained in any amount, but usually the content is the total amount of the oil composition. It is desirable that the content is 0.01 to 1% by mass.

  Specific examples of the metal deactivator include imidazole compounds as well as the benzotriazole compounds mentioned as the component (K). In the present invention, one or two or more compounds arbitrarily selected from these metal deactivators can be contained in any amount, but usually the content is determined by the oil composition. It is desirable that it is 0.001-1 mass% on the basis of the total amount of things.

  As the viscosity index improver other than the dispersion type viscosity index improver (C), specifically, a copolymer of one or more monomers selected from various methacrylates or a hydrogenated product thereof, Ethylene-α-olefin copolymer (propylene, 1-butene, 1-pentene and the like can be exemplified as α-olefin) or a hydride thereof, polyisobutylene or a hydrogenated product thereof, a styrene-diene hydrogenated copolymer, and Examples include so-called non-dispersed viscosity index improvers such as polyalkylstyrene. Examples of the detergent dispersant other than the dispersion type viscosity index improver (C) include alkenyl succinimide, sulfonate, salicylate, phenate and the like. One or two or more compounds arbitrarily selected from these viscosity index improvers and detergent dispersants can be contained in any amount, but the content is usually the total amount of the oil composition. It is desirable that the content is 0.01 to 10% by mass.

  Specific examples of the pour point depressant include copolymers of one or more monomers selected from various acrylic esters and methacrylic esters or hydrogenated products thereof. One kind or two or more kinds of compounds arbitrarily selected from these pour point depressants can be contained in any amount, and the content is usually 0.00 on the basis of the total amount of the oil composition. It is desirable that it is 01-5 mass%.

  Specific examples of the antifoaming agent include silicones such as dimethyl silicone and fluorosilicone. In the present invention, one or two or more compounds arbitrarily selected from these antifoaming agents can be contained in any amount, but usually the content is the total amount of the oil composition. It is desirable that it is 0.0001-0.05 mass% on the basis.

Use:
The lubricating oil composition for a paper machine of the present invention can be used as a lubricating oil for all sliding parts of a paper machine. Becomes prominent.

The present invention will be further described below with reference to examples and comparative examples.
The types and amounts of the tested base oils and additives added thereto are shown below. Moreover, the test method performed about each mix | blended lubricating oil composition is also shown below similarly. The obtained test results are summarized in Tables 1 to 5.

(Test method)
(Abrasion resistance: FALEX abrasion test)
In the FALEX wear test, the amount of wear was measured using a test machine specified in ASTM D 3233-93 “Standard Test Methods for Measurement of Extreme Pressure Properties of Fluid Lubricants (Falex Pin Vee Block Methods)”. The pin (journal) is made of steel with an outer diameter of 6.35 mm (1/4 inch) and a length of 31.75 mm (1/4 inch), and the V-shaped block is made of steel with an angle of 96 degrees. It was. The test conditions were 1000 rpm, Direct Load 100 lbs, and a test time of 16 hours.
(Thermal stability test)
In accordance with JIS K2540-1989, “Lubricant Thermal Stability Test Method”, the sludge generation inhibitory effect of the lubricant was evaluated. That is, 45 g of the lubricating oil shown in the table was placed in a 50 ml beaker, and the copper and iron catalyst were placed therein, left in an air thermostat at 150 ° C. for 120 hours, and the amount of sludge in the sample oil was measured. The amount of generated sludge was determined by diluting the lubricating oil after the test with n-hexane, filtering with a 0.8 μm membrane filter, and measuring the weight of the collected material. In addition, the copper and iron catalyst used what cut | disconnected the catalyst used for a turbine oil oxidation stability test (JIS K2514) into 8 volumes (about 3.5 cm in length).
(Corrosion prevention: Rust prevention test)
The rust prevention test was carried out by a test method improved in order to evaluate the anticorrosion property of the lubricating oil for paper machines, according to JIS K 2510 “Testing method for lubricating oil rust prevention performance”. Changes were made when distilled water or artificial seawater was used when evaluating normal lubricating oil, but when evaluating lubricating oil for paper machines, artificial white water was used instead of these, and the test time was 2 hours.

(Base oil)
Base oil 1: solvent refined paraffinic mineral oil (kinematic viscosity 220mm ² / s (40 ° C), viscosity index 95)
Base oil 2: 1-decene oligomer (kinematic viscosity 220mm ² / s (40 ° C), viscosity index 140)
Base oil 3: Polyol ester obtained by using a mixture of pentaerythritol and dipentaerythritol and a linear saturated fatty acid having 5 to 12 carbon atoms (kinematic viscosity 220 mm ² / s (40 ° C.), viscosity index 120)

(Additive)
(A) Component A1: β-dithiophosphorylated propionic acid A2: β-dithiophosphorylated propionic acid ethyl ester (B) Component B1: Triphenylphosphorothionate (C) Component C1: C1-C18 alkyl methacrylate ( 90mol%) and morpholinoethyl methacrylate (10mol%) copolymer (number average molecular weight 80,000)
C2: Copolymer of C1-C18 alkyl methacrylate (90 mol%) and benzoylamino methacrylate (10 mol%) (number average molecular weight 70,000)
(D) Component D1: N-oleoyl sarcosine (E) Component E1: Nonylphenoxyacetic acid (NPA)
(F) Component F1: 2,5-bis (n-nonyldithio) -1,3,4-thiadiazole F2: zinc dioctyldithiophosphate (ZnDTP)
Other additives Amine: Dioctyldiphenylamine DBPC: Di-tertbutyl-p-cresol TCP: tricresyl phosphate

Claims (1)

Base oil is at least one selected from mineral oil, fat and synthetic oil,
(A) phosphorus-containing carboxylic acid compound and / or (B) phosphorothioate,
A lubricating oil composition for a paper machine, comprising: